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Avella of Deer Valley, Inc. Store 38
Avella of Deer Valley, Inc. Store 38: 50 FDA recall reports
Every drug recall the FDA has published for Avella of Deer Valley, Inc. Store 38. The fault, and how the agency graded it.
50Reports
0Class I
0Ongoing
2019-10-30Most recent
What the classes mean
The FDA sorts every recall into one of three classes. The class is the whole story. It is also the part people skip.
Class II is the bulk of every list here. That matters. A long list of Class II says something different from one Class I.
By class
By year reported
Checking whether it affects you
The lot or code number is what matters. Not the product name. A recall covers
specific lots. Yours may not be one of them.
Check the code on your package against the report. The FDA keeps the current
list at fda.gov/safety/recalls.
The reports
The text below is quoted from the FDA record word for word.
Povidone Iodine, 5% Ophthalmic Solution, 5 mL per droptainer, Repackaged by: Avella Specialty Pharmacy, 24416
D-0152-2020 · Class II · reported 2019-10-30 · Terminated
- Why it was recalled
- Lack of sterility assurance.
- Product
- Povidone Iodine, 5% Ophthalmic Solution, 5 mL per droptainer, Repackaged by: Avella Specialty Pharmacy, 24416 N. 19th Ave., Phoenix, AZ 85085. NDC 42852-006-20
- Where it went
- Nationwide within the United States
- How much
- 808 droptainers
Bevacizumab 2.5 mg/0.1 mL, packaged in a Prefilled Syringe, Rx only, AVELLA SPECIALTY PHARMACY 24416 N. 19TH A
D-1308-2019 · Class II · reported 2019-06-05 · Terminated
- Why it was recalled
- Lack of assurance of sterility
- Product
- Bevacizumab 2.5 mg/0.1 mL, packaged in a Prefilled Syringe, Rx only, AVELLA SPECIALTY PHARMACY 24416 N. 19TH AVENUE PHOENIX, AZ 85085, NDC 42852-001-27
- Where it went
- U.S.A. nationwide
- How much
- 730 syringes
MAGnesium 2 gm sulfate, added to NS 50 mL, Sterile single use bag, 54 mL, Compounded by Avella Specialty Pharm
D-1000-2019 · Class II · reported 2019-02-20 · Terminated
- Why it was recalled
- Labeling: Incorrect or Missing Lot and/or Exp Date:The product labels contain a Two-Dimensional ( 2D ) barcode that, when scanned, reveals information specific to the batch of the labeled product, including Expiration Date. The expiration date included within these 2D barcodes is incorrect and does not match the correct expiration date listed on the face of the label itself.
- Product
- MAGnesium 2 gm sulfate, added to NS 50 mL, Sterile single use bag, 54 mL, Compounded by Avella Specialty Pharmacy 24416 N 19 th Avenue, Phoenix, AZ 85085 (877) 794-0404, NDC 42852-907-05.
- Where it went
- Distribution to 13 states: Alabama, Arizona, California, Colorado, Florida, Idaho, Michigan, Minnesota, North Carolina, New Jersey, Oregon, Pennsylvania, Texas.
- How much
- 8,500 54 mL bags
Labetalol 20mg, HCL, USP Injectable Solution, 20mg/4mL (5 mg per mL), 4mL single use syringe. Repackaged by Av
D-0997-2019 · Class II · reported 2019-02-20 · Terminated
- Why it was recalled
- Labeling: Incorrect or Missing Lot and/or Exp Date:The product labels contain a Two-Dimensional ( 2D ) barcode that, when scanned, reveals information specific to the batch of the labeled product, including Expiration Date. The expiration date included within these 2D barcodes is incorrect and does not match the correct expiration date listed on the face of the label itself.
- Product
- Labetalol 20mg, HCL, USP Injectable Solution, 20mg/4mL (5 mg per mL), 4mL single use syringe. Repackaged by Avella Specialty Pharmacy 24416 N 19th Avenue, Phoenix, AZ 85085 (877) 794-0404, NDC 42852-822-71.
- Where it went
- Distribution to 13 states: Alabama, Arizona, California, Colorado, Florida, Idaho, Michigan, Minnesota, North Carolina, New Jersey, Oregon, Pennsylvania, Texas.
- How much
- 2,840 4mL syringes
MAGnesium 1gm sulfate, added to D5W 50 mL, Volume 52 mL, sterile single use bag, Compounded by Avella Special
D-0998-2019 · Class II · reported 2019-02-20 · Terminated
- Why it was recalled
- Labeling: Incorrect or Missing Lot and/or Exp Date:The product labels contain a Two-Dimensional ( 2D ) barcode that, when scanned, reveals information specific to the batch of the labeled product, including Expiration Date. The expiration date included within these 2D barcodes is incorrect and does not match the correct expiration date listed on the face of the label itself.
- Product
- MAGnesium 1gm sulfate, added to D5W 50 mL, Volume 52 mL, sterile single use bag, Compounded by Avella Specialty Pharmacy 24416 N 19th Avenue, Phoenix, AZ 85085 (877) 794-0404, NDC 42852-901-05.
- Where it went
- Distribution to 13 states: Alabama, Arizona, California, Colorado, Florida, Idaho, Michigan, Minnesota, North Carolina, New Jersey, Oregon, Pennsylvania, Texas.
- How much
- 250 52 mL bags
MAGnesium 2gm sulfate, added to D5W 50 mL, Volume: 54 mL, Sterile single use bag, Compounded by Avella Specia
D-0999-2019 · Class II · reported 2019-02-20 · Terminated
- Why it was recalled
- Labeling: Incorrect or Missing Lot and/or Exp Date:The product labels contain a Two-Dimensional ( 2D ) barcode that, when scanned, reveals information specific to the batch of the labeled product, including Expiration Date. The expiration date included within these 2D barcodes is incorrect and does not match the correct expiration date listed on the face of the label itself.
- Product
- MAGnesium 2gm sulfate, added to D5W 50 mL, Volume: 54 mL, Sterile single use bag, Compounded by Avella Specialty Pharmacy 24416 N 19th Avenue, Phoenix, AZ 85085 (877) 794-0404, NDC 42852-902-05.
- Where it went
- Distribution to 13 states: Alabama, Arizona, California, Colorado, Florida, Idaho, Michigan, Minnesota, North Carolina, New Jersey, Oregon, Pennsylvania, Texas.
- How much
- 4,950 54 mL bags
BEVACIZUMAB 2.5 MG/0.1ML, pre-filled syringe (deliverable dose of 1.25MG in normject syringe) Repackaged by Av
D-0224-2019 · Class II · reported 2018-11-14 · Terminated
- Why it was recalled
- Lack of Assurance of Sterility
- Product
- BEVACIZUMAB 2.5 MG/0.1ML, pre-filled syringe (deliverable dose of 1.25MG in normject syringe) Repackaged by Avella Specialty Pharmacy, 24416 N 19th Avenue, Pheonix, AZ 85085. NDC 42852-001-24
- Where it went
- Product was distributed throughout the United States.
- How much
- 911 syringes
Phenylephrine 25 mg added to NS 250 mL Bag, Rx only, Advanced Pharma, Inc. d/b/a Avella of Houston, and Avella
D-0134-2019 · Class II · reported 2018-11-07 · Terminated
- Why it was recalled
- Lack of assurance of sterility
- Product
- Phenylephrine 25 mg added to NS 250 mL Bag, Rx only, Advanced Pharma, Inc. d/b/a Avella of Houston, and Avella of Deer Valley, Inc. #38
- Where it went
- U.S.A. nationwide.
- How much
- 300 bags
Morphine (1 mg/mL) in NS 100 mL Bag, Rx only, Advanced Pharma, Inc. d/b/a Avella of Houston, and Avella of Dee
D-0131-2019 · Class II · reported 2018-11-07 · Terminated
- Why it was recalled
- Lack of assurance of sterility
- Product
- Morphine (1 mg/mL) in NS 100 mL Bag, Rx only, Advanced Pharma, Inc. d/b/a Avella of Houston, and Avella of Deer Valley, Inc. #38
- Where it went
- U.S.A. nationwide.
- How much
- 1,360 bags
Phenylephrine 30 mg added to NS 250 mL Bag, Rx only, Advanced Pharma, Inc. d/b/a Avella of Houston, and Avella
D-0135-2019 · Class II · reported 2018-11-07 · Terminated
- Why it was recalled
- Lack of assurance of sterility
- Product
- Phenylephrine 30 mg added to NS 250 mL Bag, Rx only, Advanced Pharma, Inc. d/b/a Avella of Houston, and Avella of Deer Valley, Inc. #38
- Where it went
- U.S.A. nationwide.
- How much
- 300 bags
Fentanyl (10 mcg/mL) in NS 1 mL (in 3mL BD Syringe), Rx only, Advanced Pharma, Inc. d/b/a Avella of Houston, a
D-0132-2019 · Class II · reported 2018-11-07 · Terminated
- Why it was recalled
- Lack of assurance of sterility
- Product
- Fentanyl (10 mcg/mL) in NS 1 mL (in 3mL BD Syringe), Rx only, Advanced Pharma, Inc. d/b/a Avella of Houston, and Avella of Deer Valley, Inc. #38
- Where it went
- U.S.A. nationwide.
- How much
- 20 syringes
Hydromorphone (0.2 mg/mL) in NS 100 mL Bag, Rx only, Advanced Pharma, Inc. d/b/a Avella of Houston, and Avella
D-0133-2019 · Class II · reported 2018-11-07 · Terminated
- Why it was recalled
- Lack of assurance of sterility
- Product
- Hydromorphone (0.2 mg/mL) in NS 100 mL Bag, Rx only, Advanced Pharma, Inc. d/b/a Avella of Houston, and Avella of Deer Valley, Inc. #38
- Where it went
- U.S.A. nationwide.
- How much
- 360 bags
0.2% ROPivacaine, (Ropivacaine HCL PF, USP 500mg, 0.9% Sodium Chloride, USP QS 250 mL). Volume 250 mL. Single
D-0942-2018 · Class II · reported 2018-07-25 · Terminated
- Why it was recalled
- Lack of Assurance of Sterility: Potential leakage of bags.
- Product
- 0.2% ROPivacaine, (Ropivacaine HCL PF, USP 500mg, 0.9% Sodium Chloride, USP QS 250 mL). Volume 250 mL. Single dose Cassette. For: Parkland Memorial Hospital. By: Advanced Pharma, 9225 Kirby Dr. Houston, TX 77054. Parkland Memorial Hospital NDC 15082-002-87
- Where it went
- Nationwide in the USA
- How much
- 20 bags
fentaNYL (10 mcg per mL) in 0.95 Sodium Chloride, USP QS 1mL. Volume 1mL. Single dose Syringe. For: Hunt Regio
D-0933-2018 · Class II · reported 2018-07-25 · Terminated
- Why it was recalled
- Lack of Assurance of Sterility: Potential leakage of bags.
- Product
- fentaNYL (10 mcg per mL) in 0.95 Sodium Chloride, USP QS 1mL. Volume 1mL. Single dose Syringe. For: Hunt Regional Medical Center, By: Advanced Pharma, 9265 Kirby Dr,., Houston, TX 77054. NDC 15082-210-70
- Where it went
- Nationwide in the USA
- How much
- 120 syringes
ePHEDrine Sulfate, USP 50 mg in 0.9% Sodium Chloride, USP QS 10mL. 50 mg/10 mL (5 mg per mL). Volume 10 mL Si
D-0964-2018 · Class II · reported 2018-07-25 · Terminated
- Why it was recalled
- Lack of Assurance of Sterility: Potential leakage of bags.
- Product
- ePHEDrine Sulfate, USP 50 mg in 0.9% Sodium Chloride, USP QS 10mL. 50 mg/10 mL (5 mg per mL). Volume 10 mL Single dose syringe. Avella of Houston, 9265 Kirby Dr., Houston, TX 77054 NDC 42852-895-61
- Where it went
- Nationwide in the USA
- How much
- 225 syringes
Midazolam 0.5mg/mL (Midazolam HCL (USP) 50 mg, 0.9% Sodium Chloride, USP QS 100 mL) Volume: 100 mL. Single do
D-0956-2018 · Class II · reported 2018-07-25 · Terminated
- Why it was recalled
- Lack of Assurance of Sterility: Potential leakage of bags.
- Product
- Midazolam 0.5mg/mL (Midazolam HCL (USP) 50 mg, 0.9% Sodium Chloride, USP QS 100 mL) Volume: 100 mL. Single dose bag. For: Coral Gables Hospital, By: Advanced Pharma, 9265 Kirby Dr., Houston TX 77054. NDC 15082-408-10
- Where it went
- Nationwide in the USA
- How much
- 220 bags
HYDROmorphone 1 mg/mL (HYDROmorphone HCL (USP) 30 mg, 0.9% Sodium Chloride (USP) QS 30 mL) Volume: 30mL. Singl
D-0949-2018 · Class II · reported 2018-07-25 · Terminated
- Why it was recalled
- Lack of Assurance of Sterility: Potential leakage of bags.
- Product
- HYDROmorphone 1 mg/mL (HYDROmorphone HCL (USP) 30 mg, 0.9% Sodium Chloride (USP) QS 30 mL) Volume: 30mL. Single dose syringe. Avella of Houston, 9265 Kirby Dr., Houston, TX. NDC 42852-222-63
- Where it went
- Nationwide in the USA
- How much
- 480 syringes
ceFAZolin 2 gm in NS 100mL. ceFAZolin Sodium (USP) 2gm, 0.9% Sodium Chloride (USP) 100mL. Volume 110 mL. Singl
D-0929-2018 · Class II · reported 2018-07-25 · Terminated
- Why it was recalled
- Lack of Assurance of Sterility: Potential leakage of bags.
- Product
- ceFAZolin 2 gm in NS 100mL. ceFAZolin Sodium (USP) 2gm, 0.9% Sodium Chloride (USP) 100mL. Volume 110 mL. Single dose bag. Avella of Houston 9265 Kirby Dr., Houston, TX 77054 NDC: 42852-604-10
- Where it went
- Nationwide in the USA
- How much
- 2,500 bags
ePHEDrine Sulfate, USP 50mg in 0.9% Sodium Chloride USP QS 10mL. 50 mg/10 mL (5 mg/mL). Volume: 10 mL. Single
D-0943-2018 · Class II · reported 2018-07-25 · Terminated
- Why it was recalled
- Lack of Assurance of Sterility: Potential leakage of bags.
- Product
- ePHEDrine Sulfate, USP 50mg in 0.9% Sodium Chloride USP QS 10mL. 50 mg/10 mL (5 mg/mL). Volume: 10 mL. Single dose syringe. Avella of Houston, 9265 Kirby Dr., Houston, TX 77054. NDC 42852-891-61
- Where it went
- Nationwide in the USA
- How much
- 500 syringes
PHENYLephrine 40 mg (PHENYLephrine HCL (USP) 40 mg, 5%Dextrose Inj., USP 250 mL) Volume: 254 mL. Single dose b
D-0940-2018 · Class II · reported 2018-07-25 · Terminated
- Why it was recalled
- Lack of Assurance of Sterility: Potential leakage of bags.
- Product
- PHENYLephrine 40 mg (PHENYLephrine HCL (USP) 40 mg, 5%Dextrose Inj., USP 250 mL) Volume: 254 mL. Single dose bag. Avella of Houston, 9265 Kirby Dr., Houston, TX 77054. NDC 42852-893-25
- Where it went
- Nationwide in the USA
- How much
- 200 bags
NORepiNEPHrine 8 mg (norepinephrine Bitartrate (USP) 8 mg added to 5% Dextrose Inj. (USP) 250 mL. (Concentrati
D-0939-2018 · Class II · reported 2018-07-25 · Terminated
- Why it was recalled
- Lack of Assurance of Sterility: Potential leakage of bags.
- Product
- NORepiNEPHrine 8 mg (norepinephrine Bitartrate (USP) 8 mg added to 5% Dextrose Inj. (USP) 250 mL. (Concentration 32 mcg/mL) Volume: 258 mL. Single dose bag. Avella of Houston, 9265 Kirby Dr. Houston, TX 77054. NDC 42852-815-25
- Where it went
- Nationwide in the USA
- How much
- 4,280 bags
NORepiNEPHrine Bitartrate, USP 160 mcg in 5% Dextrose, USP QS 10mL. Volume 10mL. Single dose syringe. Avella o
D-0959-2018 · Class II · reported 2018-07-25 · Terminated
- Why it was recalled
- Lack of Assurance of Sterility: Potential leakage of bags.
- Product
- NORepiNEPHrine Bitartrate, USP 160 mcg in 5% Dextrose, USP QS 10mL. Volume 10mL. Single dose syringe. Avella of Houston, 9265 Kirby Dr. Houston, TX 77054. NDC 42852-807-61
- Where it went
- Nationwide in the USA
- How much
- 850 syringes
HEPARIN 25,000 Units in 5% Dextrose (Heparin Sodium, USP 25,000 Units, 5% Dextrose Inj., USP 250 mL) Volume: 2
D-0934-2018 · Class II · reported 2018-07-25 · Terminated
- Why it was recalled
- Lack of Assurance of Sterility: Potential leakage of bags.
- Product
- HEPARIN 25,000 Units in 5% Dextrose (Heparin Sodium, USP 25,000 Units, 5% Dextrose Inj., USP 250 mL) Volume: 255 mL. Single dose bag. Avella Specialty Pharmacy, 24416 N 19th Avenue, Pheonix AZ 85085. NDC 42852-729-25
- Where it went
- Nationwide in the USA
- How much
- 240 bags
MORphine 150 mg (Morphine Sulfate, USP 150mg in 0.9% Sodium Chloride, USP QS 30mL). Volume 30 mL. Single dose
D-0954-2018 · Class II · reported 2018-07-25 · Terminated
- Why it was recalled
- Lack of Assurance of Sterility: Potential leakage of bags.
- Product
- MORphine 150 mg (Morphine Sulfate, USP 150mg in 0.9% Sodium Chloride, USP QS 30mL). Volume 30 mL. Single dose syringe. Avella of Houston, 9265 Kirby Dr., Houston, TX 77054. NDC 42852-243-63
- Where it went
- Nationwide in the USA
- How much
- 740 syringes
HEPARIN 12,500 Units in 5% Dextrose. (Heparin Sodium, USP 12,500 Units, 5% Dextrose Inj., USP 250 mL) Volume:
D-0947-2018 · Class II · reported 2018-07-25 · Terminated
- Why it was recalled
- Lack of Assurance of Sterility: Potential leakage of bags.
- Product
- HEPARIN 12,500 Units in 5% Dextrose. (Heparin Sodium, USP 12,500 Units, 5% Dextrose Inj., USP 250 mL) Volume: 252.5 mL. Single dose bag. Avella Specialty Pharmacy, 24416 N 19th Avenue Phoenix, AZ 85085. NDC 42852-745-25
- Where it went
- Nationwide in the USA
- How much
- 900 bags
ePHEDrine Sulfate, USP 25 mg in 0.9% Sodium Chloride, USP QS 5mL. Volume 5 mL Single dose syringe. Avella of
D-0963-2018 · Class II · reported 2018-07-25 · Terminated
- Why it was recalled
- Lack of Assurance of Sterility: Potential leakage of bags.
- Product
- ePHEDrine Sulfate, USP 25 mg in 0.9% Sodium Chloride, USP QS 5mL. Volume 5 mL Single dose syringe. Avella of Houston, 9265 Kirby Dr., Houston, TX 77054 NDC 42852-805-67
- Where it went
- Nationwide in the USA
- How much
- 10500 syringes
MAGnesium 1gm in NS 100 mL (MAGnesium SULfate (USP) 1 gm, 0.9% Sodium Chloride (USP) 100 mL). Volume: 102 mL.
D-0951-2018 · Class II · reported 2018-07-25 · Terminated
- Why it was recalled
- Lack of Assurance of Sterility: Potential leakage of bags.
- Product
- MAGnesium 1gm in NS 100 mL (MAGnesium SULfate (USP) 1 gm, 0.9% Sodium Chloride (USP) 100 mL). Volume: 102 mL. Single dose bag. For: Salt Lake Regional Med Ctr By: Avella of Houston, 9256 Kirby Dr., Houston, TX 77054. NDC: 42852-906-10
- Where it went
- Nationwide in the USA
- How much
- 25 bags
Midazolam 1 mg/mL (Midazolam HCL (USP) 100 mg, Sodium Chloride, USP QS 100 mL) Volume: 100 mL. Single dose bag
D-0937-2018 · Class II · reported 2018-07-25 · Terminated
- Why it was recalled
- Lack of Assurance of Sterility: Potential leakage of bags.
- Product
- Midazolam 1 mg/mL (Midazolam HCL (USP) 100 mg, Sodium Chloride, USP QS 100 mL) Volume: 100 mL. Single dose bag. Avella of Houston, 9265 Kirby Dr., Houston TX 77054. NDC 4252-401-10
- Where it went
- Nationwide in the USA
- How much
- 1860 bags
PHENYLephrine 20 mg (PHENYLephrine HCL (USP) 20 mg, 5% Dextrose (USP) 250 mL) Volume: 252 mL. Single dose bag.
D-0962-2018 · Class II · reported 2018-07-25 · Terminated
- Why it was recalled
- Lack of Assurance of Sterility: Potential leakage of bags.
- Product
- PHENYLephrine 20 mg (PHENYLephrine HCL (USP) 20 mg, 5% Dextrose (USP) 250 mL) Volume: 252 mL. Single dose bag. For: Vidant Medical Center, By: Avella of Houston, 9265 Kirby Dr., Houston, TX 77054. NDC 42852-894-25
- Where it went
- Nationwide in the USA
- How much
- 120 bags
NORepiNEPHrine4mg (Norepinephrine Bitartrate (USP) 4 mg added to 0.9% Sodium Chloride (USP) 250 mL Volume: 254
D-0961-2018 · Class II · reported 2018-07-25 · Terminated
- Why it was recalled
- Lack of Assurance of Sterility: Potential leakage of bags.
- Product
- NORepiNEPHrine4mg (Norepinephrine Bitartrate (USP) 4 mg added to 0.9% Sodium Chloride (USP) 250 mL Volume: 254 mL Single dose bag. Avella of Houston, 9265 Kirby Dr. Houston, TX 77054. NDC 42852-860-25
- Where it went
- Nationwide in the USA
- How much
- 1290 bags
Showing the 30 most recent of 50. The rest are searchable at the FDA enforcement report database.
Read these counts with three things in mind
A firm with more recalls usually makes more products. A contract packer runs
hundreds of lines. It will out-recall a company with one product whatever either
does. This is not a safety ranking.
Most recalls here are voluntary. A firm found its own fault and pulled the stock.
That is the system working. It lands in this database looking the same as a recall
the FDA had to push for.
Terminated means the FDA considers the recall finished. It is not a verdict.
It does not mean anyone was harmed.
Source: openFDA enforcement reports, retrieved 2026-08-05. FDA dataset last updated 2026-07-29.
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