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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

Initiated in 2016. Latest and historical records, ordered by initiation date (newest first). FDA status appears on each record.

23 recall recordsPage 2 of 2
Class II
FDA status: Terminated

Poly-Vita Drops, 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

Poly-Vita Drops with Iron, 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

D-Vita Drops, 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

Ferrous Drops, 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

Tri-Vita Drops, 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

Pedia Tri-Vite Drops, 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

Pedia Tri-Vite Drops with Iron, 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

Pedia Poly-Vite Drops, 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

Pedia D-Vite Drops, 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

Renew HC, Hydrolyzed Clinoptilolite

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

Other contaminationView details →
Class II
FDA status: Terminated

CytoDetox, Hydrolyzed Clinoptilolite Fragments

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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