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RECALLING FIRM / COMPANY

Pharmatech LLC Recalls

Are there any recent recalls involving Pharmatech LLC?

0 recall records initiated in the snapshot’s last 365 days. 0 are FDA-listed ongoing with no termination date.FDA data updated September 16, 2026 · Snapshot assessed September 18, 2026

The FDA identifies this company as the recalling firm; this does not establish that it is the manufacturer, retailer or brand owner. “Recent ongoing” means initiated within 365 days of September 18, 2026, FDA status “Ongoing,” and no termination date. This snapshot cannot confirm what is active today.

42 FDA product recordsLatest initiation: Aug 16, 2017

Same product name.
Different batch.
Check the label.

All recall records involving Pharmatech LLC

Latest and historical records, ordered by initiation date (newest first). FDA status appears on each record.

42 recall recordsPage 2 of 4
Class II
FDA status: Terminated

Major Tri-Vita Drops 50 mL

Presence of yeast and potential contamination with B. cepacia.

Mold / spoilageView details →
Class II
FDA status: Terminated

Major Poly-Vita Drops w/ Iron 50 mL

Presence of yeast and potential contamination with B. cepacia.

Mold / spoilageView details →
Class II
FDA status: Terminated

Rugby Poly-Vitamin w/ Iron Liquid 50 mL

Presence of yeast and potential contamination with B. cepacia.

Mold / spoilageView details →
Class II
FDA status: Terminated

Leader Liquid Multivitamin Supplement for Infants and Toddlers 50 mL

Presence of yeast and potential contamination with B. cepacia.

Mold / spoilageView details →
Class II
FDA status: Terminated

Major Certa-Vite Liquid 236 mL

Presence of yeast and potential contamination with B. cepacia.

Mold / spoilageView details →
Class II
FDA status: Terminated

Virtrate-2, Sodium Citrate-Citric Acid, 16oz./473 mL, OTC Non-Sterile. Dietary supplement.

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

Other contaminationView details →
Class II
FDA status: Terminated

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

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

Other contaminationView details →
Class II
FDA status: Terminated

Calcionate Syrup, Calcium Glubionate Syrup

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

Other contaminationView details →
Class II
FDA status: Terminated

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

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

Other contaminationView details →
Class II
FDA status: Terminated

Cerovite Liquid

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

Other contaminationView details →
Class II
FDA status: Terminated

Ferrous Sulfate Liquid

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

Other contaminationView details →
Class II
FDA status: Terminated

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

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

Other contaminationView details →

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Same product name. Different batch. Details matter.

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