thejoe Well Care Compounding Pharmacy

Well Care Compounding Pharmacy: 51 FDA recall reports

Every drug recall the FDA has published for Well Care Compounding Pharmacy. The fault, and how the agency graded it.

51Reports

0Class I

0Ongoing

2016-06-15Most 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	What the FDA is saying
Class I	There is a reasonable probability that using this will cause serious harm or death.
Class II	It may cause temporary or reversible harm. Serious harm is unlikely.
Class III	It breaks a rule but is unlikely to hurt anyone. Often a labelling fault.

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

Class	Reports
Class II	51

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.

ESTRADIOL CYPIONATE 10 MG/ML, packaged in 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 891

D-0981-2016 · Class II · reported 2016-06-15 · Terminated

Why it was recalled: Lack of Assurance of Sterility: FDA inspection identified GMP violations potentially impacting product quality and sterility.
Product: ESTRADIOL CYPIONATE 10 MG/ML, packaged in 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
Where it went: NV
How much: 869 Units (Total All Products)

GLUTATHIONE 100MG/ML, packaged in 10 mL vials, Well Care Compounding Pharmacy Las Vegas, NV 89121

D-0986-2016 · Class II · reported 2016-06-15 · Terminated

Why it was recalled: Lack of Assurance of Sterility: FDA inspection identified GMP violations potentially impacting product quality and sterility.
Product: GLUTATHIONE 100MG/ML, packaged in 10 mL vials, Well Care Compounding Pharmacy Las Vegas, NV 89121
Where it went: NV
How much: 869 Units (Total All Products)

METHYLCOBALAMIN 1 MG/ML, packaged in 1mL and 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV

D-1000-2016 · Class II · reported 2016-06-15 · Terminated

Why it was recalled: Lack of Assurance of Sterility: FDA inspection identified GMP violations potentially impacting product quality and sterility.
Product: METHYLCOBALAMIN 1 MG/ML, packaged in 1mL and 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
Where it went: NV
How much: 869 Units (Total All Products)

QUAD-MIX #3, packaged in 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121

D-1025-2016 · Class II · reported 2016-06-15 · Terminated

Why it was recalled: Lack of Assurance of Sterility: FDA inspection identified GMP violations potentially impacting product quality and sterility.
Product: QUAD-MIX #3, packaged in 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
Where it went: NV
How much: 869 Units (Total All Products)

QUAD-MIX #2, packaged in 5mL vial, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121

D-1007-2016 · Class II · reported 2016-06-15 · Terminated

Why it was recalled: Lack of Assurance of Sterility: FDA inspection identified GMP violations potentially impacting product quality and sterility.
Product: QUAD-MIX #2, packaged in 5mL vial, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
Where it went: NV
How much: 869 Units (Total All Products)

METHYLCOBALAMIN 12.5MG/ML, packaged in 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121

D-0999-2016 · Class II · reported 2016-06-15 · Terminated

Why it was recalled: Lack of Assurance of Sterility: FDA inspection identified GMP violations potentially impacting product quality and sterility.
Product: METHYLCOBALAMIN 12.5MG/ML, packaged in 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
Where it went: NV
How much: 869 Units (Total All Products)

ITRACONAZOLE 0.2%/MUPIROCIN 0.2% NASAL SPRAY; 30 mL Spray, Rx only, Well Care Compounding Pharmacy Las Vegas,

D-1027-2016 · Class II · reported 2016-06-15 · Terminated

Why it was recalled: Lack of Assurance of Sterility: FDA inspection identified GMP violations potentially impacting product quality and sterility.
Product: ITRACONAZOLE 0.2%/MUPIROCIN 0.2% NASAL SPRAY; 30 mL Spray, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
Where it went: NV
How much: 916 total units

MYERS' COCKTAIL, packaged in 37 mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121

D-1003-2016 · Class II · reported 2016-06-15 · Terminated

Why it was recalled: Lack of Assurance of Sterility: FDA inspection identified GMP violations potentially impacting product quality and sterility.
Product: MYERS' COCKTAIL, packaged in 37 mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
Where it went: NV
How much: 869 Units (Total All Products)

SUPER TRI-MIX #4, packaged in 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121

D-1010-2016 · Class II · reported 2016-06-15 · Terminated

Why it was recalled: Lack of Assurance of Sterility: FDA inspection identified GMP violations potentially impacting product quality and sterility.
Product: SUPER TRI-MIX #4, packaged in 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
Where it went: NV
How much: 869 Units (Total All Products)

ALPHA LIPOIC ACID 25MG/ML, packaged in 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121

D-0979-2016 · Class II · reported 2016-06-15 · Terminated

Why it was recalled: Lack of Assurance of Sterility: FDA inspection identified GMP violations potentially impacting product quality and sterility.
Product: ALPHA LIPOIC ACID 25MG/ML, packaged in 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
Where it went: NV
How much: 869 Units (Total All Products)

TRI-MIX # 1, packaged in 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121

D-1016-2016 · Class II · reported 2016-06-15 · Terminated

Why it was recalled: Lack of Assurance of Sterility: FDA inspection identified GMP violations potentially impacting product quality and sterility.
Product: TRI-MIX # 1, packaged in 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
Where it went: NV
How much: 869 Units (Total All Products)

CLOTRIMAZOLE 1%/ BETAMETHASONE DIPROPIONATE 0.05% OTIC SOLUTION, 15mL dropper, Rx only, Well Care Compounding

D-1026-2016 · Class II · reported 2016-06-15 · Terminated

Why it was recalled: Lack of Assurance of Sterility: FDA inspection identified GMP violations potentially impacting product quality and sterility.
Product: CLOTRIMAZOLE 1%/ BETAMETHASONE DIPROPIONATE 0.05% OTIC SOLUTION, 15mL dropper, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
Where it went: NV
How much: 916 total

METHYLCOBALAMIN 5MG/ML, packaged in 1mL and 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 8

D-1001-2016 · Class II · reported 2016-06-15 · Terminated

Why it was recalled: Lack of Assurance of Sterility: FDA inspection identified GMP violations potentially impacting product quality and sterility.
Product: METHYLCOBALAMIN 5MG/ML, packaged in 1mL and 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
Where it went: NV
How much: 869 Units (Total All Products)

VITAMIN B COMPLEX # 1; packaged in 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121

D-1023-2016 · Class II · reported 2016-06-15 · Terminated

Why it was recalled: Lack of Assurance of Sterility: FDA inspection identified GMP violations potentially impacting product quality and sterility.
Product: VITAMIN B COMPLEX # 1; packaged in 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
Where it went: NV
How much: 869 Units (Total All Products)

SUPER TRI-MIX #1, packaged in 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121

D-1009-2016 · Class II · reported 2016-06-15 · Terminated

Why it was recalled: Lack of Assurance of Sterility: FDA inspection identified GMP violations potentially impacting product quality and sterility.
Product: SUPER TRI-MIX #1, packaged in 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
Where it went: NV
How much: 869 Units (Total All Products)

TRI-MIX # 4, packaged in 5 mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121

D-1019-2016 · Class II · reported 2016-06-15 · Terminated

Why it was recalled: Lack of Assurance of Sterility: FDA inspection identified GMP violations potentially impacting product quality and sterility.
Product: TRI-MIX # 4, packaged in 5 mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
Where it went: NV
How much: 869 Units (Total All Products)

VITAMIN B COMPLEX # 3, packaged in 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121

D-1024-2016 · Class II · reported 2016-06-15 · Terminated

Why it was recalled: Lack of Assurance of Sterility: FDA inspection identified GMP violations potentially impacting product quality and sterility.
Product: VITAMIN B COMPLEX # 3, packaged in 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
Where it went: NV
How much: 869 Units (Total All Products)

VANCOMYCIN 50MG/ML OPHTH SOLUTION; packaged in 10mL vial, Rx only, Well Care Compounding Pharmacy Las Vegas, N

D-1022-2016 · Class II · reported 2016-06-15 · Terminated

Why it was recalled: Lack of Assurance of Sterility: FDA inspection identified GMP violations potentially impacting product quality and sterility.
Product: VANCOMYCIN 50MG/ML OPHTH SOLUTION; packaged in 10mL vial, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
Where it went: NV
How much: 869 Units (Total All Products)

L-GLUT/L-ARG/L-CARN; 25MG/100MG/200MG/ML, packaged in 5mL vials, Rx only, Well Care Compounding Pharmacy Las

D-0993-2016 · Class II · reported 2016-06-15 · Terminated

Why it was recalled: Lack of Assurance of Sterility: FDA inspection identified GMP violations potentially impacting product quality and sterility.
Product: L-GLUT/L-ARG/L-CARN; 25MG/100MG/200MG/ML, packaged in 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
Where it went: NV
How much: 869 Units (Total All Products)

GLUTATHIONE 200MG/ML, packaged in 5mL vials, Well Care Compounding Pharmacy Las Vegas, NV 89121

D-0987-2016 · Class II · reported 2016-06-15 · Terminated

Why it was recalled: Lack of Assurance of Sterility: FDA inspection identified GMP violations potentially impacting product quality and sterility.
Product: GLUTATHIONE 200MG/ML, packaged in 5mL vials, Well Care Compounding Pharmacy Las Vegas, NV 89121
Where it went: NV
How much: 869 Units (Total All Products)

M.l.C. 25MG/50MG/25MG/ML, packaged in 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121

D-0994-2016 · Class II · reported 2016-06-15 · Terminated

Why it was recalled: Lack of Assurance of Sterility: FDA inspection identified GMP violations potentially impacting product quality and sterility.
Product: M.l.C. 25MG/50MG/25MG/ML, packaged in 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
Where it went: NV
How much: 869 Units (Total All Products)

TRI-MIX # 2, packaged in 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121

D-1017-2016 · Class II · reported 2016-06-15 · Terminated

Why it was recalled: Lack of Assurance of Sterility: FDA inspection identified GMP violations potentially impacting product quality and sterility.
Product: TRI-MIX # 2, packaged in 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
Where it went: NV
How much: 869 Units (Total All Products)

METHYLCOBALAMIN/FOLIC ACID; 10MG/0.8MG/ML, packaged in 1mL and 5mL vials, Rx only, Well Care Compounding Pharm

D-1002-2016 · Class II · reported 2016-06-15 · Terminated

Why it was recalled: Lack of Assurance of Sterility: FDA inspection identified GMP violations potentially impacting product quality and sterility.
Product: METHYLCOBALAMIN/FOLIC ACID; 10MG/0.8MG/ML, packaged in 1mL and 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
Where it went: NV
How much: 869 Units (Total All Products)

M.l.C./B5/B6 25 MG/50MG/25MG/10MG/10MG/ML, packaged in 5mL vials, Rx only, Well Care Compounding Pharmacy Las

D-0998-2016 · Class II · reported 2016-06-15 · Terminated

Why it was recalled: Lack of Assurance of Sterility: FDA inspection identified GMP violations potentially impacting product quality and sterility.
Product: M.l.C./B5/B6 25 MG/50MG/25MG/10MG/10MG/ML, packaged in 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
Where it went: NV
How much: N/A

GENTAMICIN 15 MG/ML Ophthalmic Solution, Sterile Droppers, Rx only, Well Care Compounding Pharmacy Las Vegas,

D-0985-2016 · Class II · reported 2016-06-15 · Terminated

Why it was recalled: Lack of Assurance of Sterility: FDA inspection identified GMP violations potentially impacting product quality and sterility.
Product: GENTAMICIN 15 MG/ML Ophthalmic Solution, Sterile Droppers, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
Where it went: NV
How much: 869 Units (Total All Products)

17-0H PROGESTERONE 250MG/ML, packaged in 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 8912

D-0978-2016 · Class II · reported 2016-06-15 · Terminated

Why it was recalled: Lack of Assurance of Sterility: FDA inspection identified GMP violations potentially impacting product quality and sterility.
Product: 17-0H PROGESTERONE 250MG/ML, packaged in 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
Where it went: NV
How much: 869 units (total all products)

1-HCG 2000 IU/ML, packaged in 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121

D-0989-2016 · Class II · reported 2016-06-15 · Terminated

Why it was recalled: Lack of Assurance of Sterility: FDA inspection identified GMP violations potentially impacting product quality and sterility.
Product: 1-HCG 2000 IU/ML, packaged in 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
Where it went: NV
How much: 869 Units (Total All Products)

HCG/METHYLCOBALAMIN/FOLIC ACID,1000IU/5MG/0.4MG/ML; packaged in 5 mL vials, Rx only, Well Care Compounding Ph

D-0990-2016 · Class II · reported 2016-06-15 · Terminated

Why it was recalled: Lack of Assurance of Sterility: FDA inspection identified GMP violations potentially impacting product quality and sterility.
Product: HCG/METHYLCOBALAMIN/FOLIC ACID,1000IU/5MG/0.4MG/ML; packaged in 5 mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
Where it went: NV
How much: 869 Units (Total All Products)

TRI-MIX # 6, packaged in 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121

D-1021-2016 · Class II · reported 2016-06-15 · Terminated

Why it was recalled: Lack of Assurance of Sterility: FDA inspection identified GMP violations potentially impacting product quality and sterility.
Product: TRI-MIX # 6, packaged in 5mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
Where it went: NV
How much: 869 Units (Total All Products)

PHOSPHATIDYLCHOLINE/DEOXYCHOLIC ACID- 5%/4.75%, packaged in 10mL vials, Rx only, Well Care Compounding Pharma

D-1005-2016 · Class II · reported 2016-06-15 · Terminated

Why it was recalled: Lack of Assurance of Sterility: FDA inspection identified GMP violations potentially impacting product quality and sterility.
Product: PHOSPHATIDYLCHOLINE/DEOXYCHOLIC ACID- 5%/4.75%, packaged in 10mL vials, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
Where it went: NV
How much: 869 Units (Total All Products)

Showing the 30 most recent of 51. 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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