Pharmatech Llc — FDA Recall History & Enforcement Records
Data Notice: Recall frequency varies by category and firm size; data is comparative and may not indicate actual brand safety or quality. See Methodology.
As of July 16, 2026, Pharmatech Llc has 42 recorded FDA food enforcement actions in the openFDA database. Their most recent recall was on 16 Aug 2017. Pharmatech Llc is categorized under Supplements & Specialty based on their predominant recall history.
42
Total FDA recalls
11.4
Years in FDA database
3.7
Recalls per year
3,256 days(8.9 yrs)
Since last recall
0.0%
Class I (life-threatening)
3.7 recalls/yr vs Supplements & Specialty avg 2.3/yrWell Above Average
Recall activity over time for Pharmatech Llc
How serious are Pharmatech Llc recalls?
FDA recall classifications by severity
Class I (Life-threatening)
0.0% (0 recalls)
Class II (Moderate risk)
100.0% (42 recalls)
Class III (Minor violation)
0.0% (0 recalls)
Full FDA recall history for Pharmatech Llc
All 42 FDA enforcement actions sourced from openFDA · Sorted by date, most recent first
| Date | Product | Reason | Class & Status |
|---|---|---|---|
| 16 Aug 2017Official FDA Notice | Rugby FER Iron Liquid 50 mL UPC 00536-0710-80 | Presence of yeast and potential contamination with B. cepacia. | Class IITerminated |
| 16 Aug 2017Official FDA Notice | Leader Liquid Multivitamin Supplement for Infants and Toddlers 50 mL UPC 096295128611 | Presence of yeast and potential contamination with B. cepacia. | Class IITerminated |
| 16 Aug 2017Official FDA Notice | Major Poly-Vita Drops 50 mL UPC 00904-5099-50 | Presence of yeast and potential contamination with B. cepacia. | Class IITerminated |
| 16 Aug 2017Official FDA Notice | Rugby Ferrous Sulfate Elixir 473 mL UPC: 00536-0650-85 | Presence of yeast and potential contamination with B. cepacia. | Class IITerminated |
| 16 Aug 2017Official FDA Notice | Major Certa-Vite Liquid 236 mL UPC 00904-5023-09 | Presence of yeast and potential contamination with B. cepacia. | Class IITerminated |
| 16 Aug 2017Official FDA Notice | Rugby Calcionate Syrup 16 oz. UPC 00536-2770-85 | Presence of yeast and potential contamination with B. cepacia. | Class IITerminated |
| 16 Aug 2017Official FDA Notice | Leader Liquid Vitamin D Supplement for Breastfed Infants 400 IU 50 mL UPC 096295128628 | Presence of yeast and potential contamination with B. cepacia. | Class IITerminated |
| 16 Aug 2017Official FDA Notice | Rugby Polyvitamin Liquid 1 2/3 fl. oz. (50 mL) UPC 00536-8450-80 | Presence of yeast and potential contamination with B. cepacia. | Class IITerminated |
| 16 Aug 2017Official FDA Notice | Major Tri-Vita Drops 50 mL UPC 00904-6274-50 | Presence of yeast and potential contamination with B. cepacia. | Class IITerminated |
| 16 Aug 2017Official FDA Notice | Major Ferrous Drop Iron Supplement 50 mL UPC 00904-6060-50 | Presence of yeast and potential contamination with B. cepacia. | Class IITerminated |
| 16 Aug 2017Official FDA Notice | Major D-Vita Drops 50 mL UPC 00904-6273-50 | Presence of yeast and potential contamination with B. cepacia. | Class IITerminated |
| 16 Aug 2017Official FDA Notice | Rugby D3 Vitamin liquid 400 IU/1 mL dose 1 2/3 fl. oz. (50 mL) UPC 00536-8400-80 | Presence of yeast and potential contamination with B. cepacia. | Class IITerminated |
| 16 Aug 2017Official FDA Notice | Rugby Tri-Vitamin Liquid 1 2/3 fl. oz. (50 mL) UPC 00536-8501-80 | Presence of yeast and potential contamination with B. cepacia. | Class IITerminated |
| 16 Aug 2017Official FDA Notice | Rugby Liquid Vitamin C Supplement 500 mg 118 mL UPC 00536-0160-97 | Presence of yeast and potential contamination with B. cepacia. | Class IITerminated |
| 16 Aug 2017Official FDA Notice | Major Poly-Vita Drops w/ Iron 50 mL UPC 00904-5100-50 | Presence of yeast and potential contamination with B. cepacia. | Class IITerminated |
| 16 Aug 2017Official FDA Notice | Rugby Cerovite Liquid 236 mL UPC 00536-2790-59 | Presence of yeast and potential contamination with B. cepacia. | Class IITerminated |
| 16 Aug 2017Official FDA Notice | Rugby Poly-Vitamin w/ Iron Liquid 50 mL UPC 00536-8530-80 | Presence of yeast and potential contamination with B. cepacia. | Class IITerminated |
| 8 Aug 2016Official FDA Notice | CytoDetox, Hydrolyzed Clinoptilolite Fragments, 1 oz./30 mL, OTC Non-Sterile. Dietary supplement. | Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia. | Class IITerminated |
| 8 Aug 2016Official FDA Notice | 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. | Class IITerminated |
| 8 Aug 2016Official FDA Notice | 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. | Class IITerminated |
| 8 Aug 2016Official FDA Notice | 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. | Class IITerminated |
| 8 Aug 2016Official FDA Notice | 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. | Class IITerminated |
| 8 Aug 2016Official FDA Notice | Polyvitamin Liquid, 50 mL, OTC Non-Sterile. Dietary supplement. | Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia. | Class IITerminated |
| 8 Aug 2016Official FDA Notice | 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. | Class IITerminated |
| 8 Aug 2016Official FDA Notice | 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. | Class IITerminated |
| 8 Aug 2016Official FDA Notice | 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. | Class IITerminated |
| 8 Aug 2016Official FDA Notice | Renew HC, Hydrolyzed Clinoptilolite, 1 oz./30 mL, OTC Non-Sterile. Dietary supplement. | Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia. | Class IITerminated |
| 8 Aug 2016Official FDA Notice | 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. | Class IITerminated |
| 8 Aug 2016Official FDA Notice | Polyvitamin Liquid 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. | Class IITerminated |
| 8 Aug 2016Official FDA Notice | 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. | Class IITerminated |
| 8 Aug 2016Official FDA Notice | 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. | Class IITerminated |
| 8 Aug 2016Official FDA Notice | Liquid Vitamin C, 4 oz./118 mL, OTC Non-Sterile. Dietary supplement. | Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia. | Class IITerminated |
| 8 Aug 2016Official FDA Notice | Calcionate Syrup, Calcium Glubionate Syrup, 16 oz./473 mL, OTC Non-Sterile. Dietary supplement. | Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia. | Class IITerminated |
| 8 Aug 2016Official FDA Notice | 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. | Class IITerminated |
| 8 Aug 2016Official FDA Notice | 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. | Class IITerminated |
| 8 Aug 2016Official FDA Notice | CertaVite with Antioxidants, 8 oz./236 mL, OTC Non-Sterile. Dietary supplement. | Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia. | Class IITerminated |
| 8 Aug 2016Official FDA Notice | Ferrous Sulfate Liquid, 16 oz./473 mL, OTC Non-Sterile. Dietary supplement. | Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia. | Class IITerminated |
| 8 Aug 2016Official FDA Notice | Cerovite Liquid, 8 oz./236 mL, OTC Non-Sterile. Dietary supplement. | Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia. | Class IITerminated |
| 8 Aug 2016Official FDA Notice | 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. | Class IITerminated |
| 8 Aug 2016Official FDA Notice | Tri-Vitamin, 50 mL, OTC Non-Sterile. Dietary supplement. | Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia. | Class IITerminated |
| 9 Mar 2015Official FDA Notice | Rugby Poly Vitamin Liquid with Iron, 50 ml | Packaging label does not match individual product labeling. Outside packaging may have incorrect Lot/Exp and product identity. | Class IITerminated |
| 9 Mar 2015Official FDA Notice | Rugby Poly Vitamin Liquid, 50ml | Packaging label does not match individual product labeling. Outside packaging may have incorrect Lot/Exp and product identity. | Class IITerminated |
Where have Pharmatech Llc recalls occurred?
States affected across all recorded FDA enforcement actions
AL, AR, AZ, CA, CO, CT, FL, GA, HI, IL, IN, KY, LA, MA, MI, MN, MO, MS, NC, ND, NE, NH, NJ, NY, OH, OK, OR, PA, PR, SC, TN, TX, UT, VA, VT, WA, WI
Where does this recall data come from?
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Data sourced from the FDA Recall Enterprise System via openFDA API. This information is for educational purposes only and does not constitute health or legal advice. FoodRecallFinder.com is not affiliated with or endorsed by the U.S. Food and Drug Administration.
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