thejoe Pharmatech LLC

Pharmatech LLC: 42 FDA recall reports

Every food recall the FDA has published for Pharmatech LLC. The fault, and how the agency graded it.

42Reports

0Class I

0Ongoing

2018-01-31Most 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	42

By year reported

Year	Reports
2015	2
2016	23
2018	17

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.

Rugby FER Iron Liquid 50 mL UPC 00536-0710-80

F-0622-2018 · Class II · reported 2018-01-31 · Terminated

Why it was recalled: Presence of yeast and potential contamination with B. cepacia.
Product: Rugby FER Iron Liquid 50 mL UPC 00536-0710-80
Where it went: MI
How much: Unknown

Leader Liquid Multivitamin Supplement for Infants and Toddlers 50 mL UPC 096295128611

F-0635-2018 · Class II · reported 2018-01-31 · Terminated

Why it was recalled: Presence of yeast and potential contamination with B. cepacia.
Product: Leader Liquid Multivitamin Supplement for Infants and Toddlers 50 mL UPC 096295128611
Where it went: MI
How much: Unknown

Major Poly-Vita Drops 50 mL UPC 00904-5099-50

F-0630-2018 · Class II · reported 2018-01-31 · Terminated

Why it was recalled: Presence of yeast and potential contamination with B. cepacia.
Product: Major Poly-Vita Drops 50 mL UPC 00904-5099-50
Where it went: MI
How much: Unknown

Rugby Ferrous Sulfate Elixir 473 mL UPC: 00536-0650-85

F-0621-2018 · Class II · reported 2018-01-31 · Terminated

Why it was recalled: Presence of yeast and potential contamination with B. cepacia.
Product: Rugby Ferrous Sulfate Elixir 473 mL UPC: 00536-0650-85
Where it went: MI
How much: Unknown

Major Certa-Vite Liquid 236 mL UPC 00904-5023-09

F-0636-2018 · Class II · reported 2018-01-31 · Terminated

Why it was recalled: Presence of yeast and potential contamination with B. cepacia.
Product: Major Certa-Vite Liquid 236 mL UPC 00904-5023-09
Where it went: MI
How much: Unknown

Rugby Calcionate Syrup 16 oz. UPC 00536-2770-85

F-0624-2018 · Class II · reported 2018-01-31 · Terminated

Why it was recalled: Presence of yeast and potential contamination with B. cepacia.
Product: Rugby Calcionate Syrup 16 oz. UPC 00536-2770-85
Where it went: MI
How much: Unknown

Leader Liquid Vitamin D Supplement for Breastfed Infants 400 IU 50 mL UPC 096295128628

F-0627-2018 · Class II · reported 2018-01-31 · Terminated

Why it was recalled: Presence of yeast and potential contamination with B. cepacia.
Product: Leader Liquid Vitamin D Supplement for Breastfed Infants 400 IU 50 mL UPC 096295128628
Where it went: MI
How much: Unknown

Rugby Polyvitamin Liquid 1 2/3 fl. oz. (50 mL) UPC 00536-8450-80

F-0629-2018 · Class II · reported 2018-01-31 · Terminated

Why it was recalled: Presence of yeast and potential contamination with B. cepacia.
Product: Rugby Polyvitamin Liquid 1 2/3 fl. oz. (50 mL) UPC 00536-8450-80
Where it went: MI
How much: Unknown

Major Tri-Vita Drops 50 mL UPC 00904-6274-50

F-0632-2018 · Class II · reported 2018-01-31 · Terminated

Why it was recalled: Presence of yeast and potential contamination with B. cepacia.
Product: Major Tri-Vita Drops 50 mL UPC 00904-6274-50
Where it went: MI
How much: Unknown

Major Ferrous Drop Iron Supplement 50 mL UPC 00904-6060-50

F-0623-2018 · Class II · reported 2018-01-31 · Terminated

Why it was recalled: Presence of yeast and potential contamination with B. cepacia.
Product: Major Ferrous Drop Iron Supplement 50 mL UPC 00904-6060-50
Where it went: MI
How much: Unknown

Major D-Vita Drops 50 mL UPC 00904-6273-50

F-0628-2018 · Class II · reported 2018-01-31 · Terminated

Why it was recalled: Presence of yeast and potential contamination with B. cepacia.
Product: Major D-Vita Drops 50 mL UPC 00904-6273-50
Where it went: MI
How much: Unknown

Rugby D3 Vitamin liquid 400 IU/1 mL dose 1 2/3 fl. oz. (50 mL) UPC 00536-8400-80

F-0626-2018 · Class II · reported 2018-01-31 · Terminated

Why it was recalled: Presence of yeast and potential contamination with B. cepacia.
Product: Rugby D3 Vitamin liquid 400 IU/1 mL dose 1 2/3 fl. oz. (50 mL) UPC 00536-8400-80
Where it went: MI
How much: Unknown

Rugby Tri-Vitamin Liquid 1 2/3 fl. oz. (50 mL) UPC 00536-8501-80

F-0631-2018 · Class II · reported 2018-01-31 · Terminated

Why it was recalled: Presence of yeast and potential contamination with B. cepacia.
Product: Rugby Tri-Vitamin Liquid 1 2/3 fl. oz. (50 mL) UPC 00536-8501-80
Where it went: MI
How much: Unknown

Rugby Liquid Vitamin C Supplement 500 mg 118 mL UPC 00536-0160-97

F-0620-2018 · Class II · reported 2018-01-31 · Terminated

Why it was recalled: Presence of yeast and potential contamination with B. cepacia.
Product: Rugby Liquid Vitamin C Supplement 500 mg 118 mL UPC 00536-0160-97
Where it went: MI
How much: Unknown

Major Poly-Vita Drops w/ Iron 50 mL UPC 00904-5100-50

F-0633-2018 · Class II · reported 2018-01-31 · Terminated

Why it was recalled: Presence of yeast and potential contamination with B. cepacia.
Product: Major Poly-Vita Drops w/ Iron 50 mL UPC 00904-5100-50
Where it went: MI
How much: Unknown

Rugby Cerovite Liquid 236 mL UPC 00536-2790-59

F-0625-2018 · Class II · reported 2018-01-31 · Terminated

Why it was recalled: Presence of yeast and potential contamination with B. cepacia.
Product: Rugby Cerovite Liquid 236 mL UPC 00536-2790-59
Where it went: MI
How much: Unknown

Rugby Poly-Vitamin w/ Iron Liquid 50 mL UPC 00536-8530-80

F-0634-2018 · Class II · reported 2018-01-31 · Terminated

Why it was recalled: Presence of yeast and potential contamination with B. cepacia.
Product: Rugby Poly-Vitamin w/ Iron Liquid 50 mL UPC 00536-8530-80
Where it went: MI
How much: Unknown

CytoDetox, Hydrolyzed Clinoptilolite Fragments, 1 oz./30 mL, OTC Non-Sterile. Dietary supplement.

F-0276-2017 · Class II · reported 2016-11-02 · Terminated

Why it was recalled: Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.
Product: CytoDetox, Hydrolyzed Clinoptilolite Fragments, 1 oz./30 mL, OTC Non-Sterile. Dietary supplement.
Where it went: FL, MI, MS, and OH.
How much: 1,990 bottles

Poly-Vita Drops with Iron, 50 mL, OTC Non-Sterile. Dietary supplement.

F-0267-2017 · Class II · reported 2016-11-02 · Terminated

Why it was recalled: Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.
Product: Poly-Vita Drops with Iron, 50 mL, OTC Non-Sterile. Dietary supplement.
Where it went: FL, MI, MS, and OH.
How much: 47,525 bottles

D3 Vitamin Liquid, 50 mL, OTC Non-Sterile. Dietary supplement.

F-0257-2017 · Class II · reported 2016-11-02 · Terminated

Why it was recalled: Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.
Product: D3 Vitamin Liquid, 50 mL, OTC Non-Sterile. Dietary supplement.
Where it went: FL, MI, MS, and OH.
How much: 229,464 bottles

Pedia Poly-Vite Drops, 50 mL, OTC Non-Sterile. Dietary supplement.

F-0273-2017 · Class II · reported 2016-11-02 · Terminated

Why it was recalled: Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.
Product: Pedia Poly-Vite Drops, 50 mL, OTC Non-Sterile. Dietary supplement.
Where it went: FL, MI, MS, and OH.
How much: 6,600 bottles

Pedia Tri-Vite Drops with Iron, 50 mL, OTC Non-Sterile. Dietary supplement.

F-0272-2017 · Class II · reported 2016-11-02 · Terminated

Why it was recalled: Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.
Product: Pedia Tri-Vite Drops with Iron, 50 mL, OTC Non-Sterile. Dietary supplement.
Where it went: FL, MI, MS, and OH.
How much: 6,024 bottles

Polyvitamin Liquid, 50 mL, OTC Non-Sterile. Dietary supplement.

F-0262-2017 · Class II · reported 2016-11-02 · Terminated

Why it was recalled: Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.
Product: Polyvitamin Liquid, 50 mL, OTC Non-Sterile. Dietary supplement.
Where it went: FL, MI, MS, and OH.
How much: 188,640 bottles

Fer-Iron Liquid, 50 mL, OTC Non-Sterile. Dietary supplement.

F-0260-2017 · Class II · reported 2016-11-02 · Terminated

Why it was recalled: Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.
Product: Fer-Iron Liquid, 50 mL, OTC Non-Sterile. Dietary supplement.
Where it went: FL, MI, MS, and OH.
How much: 99,024 bottles

Ferrous Drops, 50 mL, OTC Non-Sterile. Dietary supplement.

F-0269-2017 · Class II · reported 2016-11-02 · Terminated

Why it was recalled: Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.
Product: Ferrous Drops, 50 mL, OTC Non-Sterile. Dietary supplement.
Where it went: FL, MI, MS, and OH.
How much: 31,224 bottles

Poly-Vita Drops, 50 mL, OTC Non-Sterile. Dietary supplement.

F-0266-2017 · Class II · reported 2016-11-02 · Terminated

Why it was recalled: Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.
Product: Poly-Vita Drops, 50 mL, OTC Non-Sterile. Dietary supplement.
Where it went: FL, MI, MS, and OH.
How much: 42,984 bottles

Renew HC, Hydrolyzed Clinoptilolite, 1 oz./30 mL, OTC Non-Sterile. Dietary supplement.

F-0275-2017 · Class II · reported 2016-11-02 · Terminated

Why it was recalled: Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.
Product: Renew HC, Hydrolyzed Clinoptilolite, 1 oz./30 mL, OTC Non-Sterile. Dietary supplement.
Where it went: FL, MI, MS, and OH.
How much: 62,228 bottles

Virtrate-K, Potassium Citrate and Citric Acid, 16oz./473 mL, OTC Non-Sterile. Dietary supplement.

F-0255-2017 · Class II · reported 2016-11-02 · Terminated

Why it was recalled: Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.
Product: Virtrate-K, Potassium Citrate and Citric Acid, 16oz./473 mL, OTC Non-Sterile. Dietary supplement.
Where it went: FL, MI, MS, and OH.
How much: 8,232 bottles

Polyvitamin Liquid with Iron, 50 mL, OTC Non-Sterile. Dietary supplement.

F-0261-2017 · Class II · reported 2016-11-02 · Terminated

Why it was recalled: Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.
Product: Polyvitamin Liquid with Iron, 50 mL, OTC Non-Sterile. Dietary supplement.
Where it went: FL, MI, MS, and OH.
How much: 201,784 bottles

D-Vita Drops, 50 mL, OTC Non-Sterile. Dietary supplement.

F-0268-2017 · Class II · reported 2016-11-02 · Terminated

Why it was recalled: Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.
Product: D-Vita Drops, 50 mL, OTC Non-Sterile. Dietary supplement.
Where it went: FL, MI, MS, and OH.
How much: 90,504 bottles

Showing the 30 most recent of 42. 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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