Pharmatech LLC FDA recall records
The FDA has published 42 food recall enforcement records naming Pharmatech LLC between 2015 and 2018, covering 3 separate recall events. The firm is recorded in Florida. Data last updated 2 September 2026.

- Records of 29,386
- 42
- Share of all recalls
- 0.1%
- Class I of 42
- 0
- Reported between
- 2015 to 2018
What is different about Pharmatech LLC
The hazard that separates Pharmatech LLC from the national picture is spoilage and mould: 40.5% of these records name it, against 2.7% of all FDA food recalls.
By product, Pharmatech LLC is weighted toward dietary supplements: 78.6% of the records here against 6.2% across the corpus.
Recalls at Pharmatech LLC skew less severe than the corpus: 0% are Class I against 44% nationally.
A recall at Pharmatech LLC stays open a median of 2,968 days between the report and termination, against 215 days for the corpus as a whole. Termination follows the firm accounting for every unit of the affected lot.
These recalls stay local: 0% state nationwide distribution, against 20.7% across the corpus.
A single recall here covers far more records than usual: 14 enforcement records per FDA event, against 3.7 across the corpus. The agency opens one record per product code, so this is a sign of broad product lines rather than of repeated failures.
What these records are
Every record on this page was published by the FDA in the openFDA food enforcement database. 42 records cover 3 recall events, because the agency opens one record per product code: a single recall of a product line with many codes appears here many times.
0 of these records are Class I, 42 Class II and 0 Class III. A recall count is not a safety score. Most FDA food recalls are initiated by the firm itself, and a recall is the firm removing product from the market, which is what a food safety plan is built to produce.
What was recalled for
A single record can name more than one hazard, so these counts overlap.
By year
Counts are by the date the FDA reported the enforcement action. That date runs behind the date a firm started a recall, so the most recent year is always partial.
Where the recalling firms are
The state is the location of the recalling firm, not where the product was sold. Distribution is recorded separately on each record.
Most recently reported
| Reported | Product | Firm | Reason | Class |
|---|---|---|---|---|
| 2018-01-31 | Rugby FER Iron Liquid 50 mL UPC 00536-0710-80 | Pharmatech LLC | Presence of yeast and potential contamination with B. cepacia. | Class II |
| 2018-01-31 | Leader Liquid Multivitamin Supplement for Infants and Toddlers 50 mL UPC 096295128611 | Pharmatech LLC | Presence of yeast and potential contamination with B. cepacia. | Class II |
| 2018-01-31 | Major Poly-Vita Drops 50 mL UPC 00904-5099-50 | Pharmatech LLC | Presence of yeast and potential contamination with B. cepacia. | Class II |
| 2018-01-31 | Rugby Ferrous Sulfate Elixir 473 mL UPC: 00536-0650-85 | Pharmatech LLC | Presence of yeast and potential contamination with B. cepacia. | Class II |
| 2018-01-31 | Major Certa-Vite Liquid 236 mL UPC 00904-5023-09 | Pharmatech LLC | Presence of yeast and potential contamination with B. cepacia. | Class II |
| 2018-01-31 | Rugby Calcionate Syrup 16 oz. UPC 00536-2770-85 | Pharmatech LLC | Presence of yeast and potential contamination with B. cepacia. | Class II |
| 2018-01-31 | Leader Liquid Vitamin D Supplement for Breastfed Infants 400 IU 50 mL UPC 096295128628 | Pharmatech LLC | Presence of yeast and potential contamination with B. cepacia. | Class II |
| 2018-01-31 | Rugby Polyvitamin Liquid 1 2/3 fl. oz. (50 mL) UPC 00536-8450-80 | Pharmatech LLC | Presence of yeast and potential contamination with B. cepacia. | Class II |
| 2018-01-31 | Major Tri-Vita Drops 50 mL UPC 00904-6274-50 | Pharmatech LLC | Presence of yeast and potential contamination with B. cepacia. | Class II |
| 2018-01-31 | Major Ferrous Drop Iron Supplement 50 mL UPC 00904-6060-50 | Pharmatech LLC | Presence of yeast and potential contamination with B. cepacia. | Class II |
| 2018-01-31 | Major D-Vita Drops 50 mL UPC 00904-6273-50 | Pharmatech LLC | Presence of yeast and potential contamination with B. cepacia. | Class II |
| 2018-01-31 | Rugby D3 Vitamin liquid 400 IU/1 mL dose 1 2/3 fl. oz. (50 mL) UPC 00536-8400-80 | Pharmatech LLC | Presence of yeast and potential contamination with B. cepacia. | Class II |
| 2018-01-31 | Rugby Tri-Vitamin Liquid 1 2/3 fl. oz. (50 mL) UPC 00536-8501-80 | Pharmatech LLC | Presence of yeast and potential contamination with B. cepacia. | Class II |
| 2018-01-31 | Rugby Liquid Vitamin C Supplement 500 mg 118 mL UPC 00536-0160-97 | Pharmatech LLC | Presence of yeast and potential contamination with B. cepacia. | Class II |
| 2018-01-31 | Major Poly-Vita Drops w/ Iron 50 mL UPC 00904-5100-50 | Pharmatech LLC | Presence of yeast and potential contamination with B. cepacia. | Class II |
| 2018-01-31 | Rugby Cerovite Liquid 236 mL UPC 00536-2790-59 | Pharmatech LLC | Presence of yeast and potential contamination with B. cepacia. | Class II |
| 2018-01-31 | Rugby Poly-Vitamin w/ Iron Liquid 50 mL UPC 00536-8530-80 | Pharmatech LLC | Presence of yeast and potential contamination with B. cepacia. | Class II |
| 2016-11-02 | CytoDetox, Hydrolyzed Clinoptilolite Fragments, 1 oz./30 mL, OTC Non-Sterile. Dietary supplement. | Pharmatech LLC | Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia. | Class II |
| 2016-11-02 | Poly-Vita Drops with Iron, 50 mL, OTC Non-Sterile. Dietary supplement. | Pharmatech LLC | Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia. | Class II |
| 2016-11-02 | D3 Vitamin Liquid, 50 mL, OTC Non-Sterile. Dietary supplement. | Pharmatech LLC | Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia. | Class II |
| 2016-11-02 | Pedia Poly-Vite Drops, 50 mL, OTC Non-Sterile. Dietary supplement. | Pharmatech LLC | Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia. | Class II |
| 2016-11-02 | Pedia Tri-Vite Drops with Iron, 50 mL, OTC Non-Sterile. Dietary supplement. | Pharmatech LLC | Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia. | Class II |
| 2016-11-02 | Polyvitamin Liquid, 50 mL, OTC Non-Sterile. Dietary supplement. | Pharmatech LLC | Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia. | Class II |
| 2016-11-02 | Fer-Iron Liquid, 50 mL, OTC Non-Sterile. Dietary supplement. | Pharmatech LLC | Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia. | Class II |
| 2016-11-02 | Ferrous Drops, 50 mL, OTC Non-Sterile. Dietary supplement. | Pharmatech LLC | Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia. | Class II |
| 2016-11-02 | Poly-Vita Drops, 50 mL, OTC Non-Sterile. Dietary supplement. | Pharmatech LLC | Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia. | Class II |
| 2016-11-02 | Renew HC, Hydrolyzed Clinoptilolite, 1 oz./30 mL, OTC Non-Sterile. Dietary supplement. | Pharmatech LLC | Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia. | Class II |
| 2016-11-02 | Virtrate-K, Potassium Citrate and Citric Acid, 16oz./473 mL, OTC Non-Sterile. Dietary supplement. | Pharmatech LLC | Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia. | Class II |
| 2016-11-02 | Polyvitamin Liquid with Iron, 50 mL, OTC Non-Sterile. Dietary supplement. | Pharmatech LLC | Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia. | Class II |
| 2016-11-02 | D-Vita Drops, 50 mL, OTC Non-Sterile. Dietary supplement. | Pharmatech LLC | Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia. | Class II |
| 2016-11-02 | Pedia Tri-Vite Drops, 50 mL, OTC Non-Sterile. Dietary supplement. | Pharmatech LLC | Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia. | Class II |
| 2016-11-02 | Liquid Vitamin C, 4 oz./118 mL, OTC Non-Sterile. Dietary supplement. | Pharmatech LLC | Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia. | Class II |
| 2016-11-02 | Calcionate Syrup, Calcium Glubionate Syrup, 16 oz./473 mL, OTC Non-Sterile. Dietary supplement. | Pharmatech LLC | Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia. | Class II |
| 2016-11-02 | Virtrate-2, Sodium Citrate-Citric Acid, 16oz./473 mL, OTC Non-Sterile. Dietary supplement. | Pharmatech LLC | Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia. | Class II |
| 2016-11-02 | Tri-Vita Drops, 50 mL, OTC Non-Sterile. Dietary supplement. | Pharmatech LLC | Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia. | Class II |
| 2016-11-02 | CertaVite with Antioxidants, 8 oz./236 mL, OTC Non-Sterile. Dietary supplement. | Pharmatech LLC | Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia. | Class II |
| 2016-11-02 | Ferrous Sulfate Liquid, 16 oz./473 mL, OTC Non-Sterile. Dietary supplement. | Pharmatech LLC | Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia. | Class II |
| 2016-11-02 | Cerovite Liquid, 8 oz./236 mL, OTC Non-Sterile. Dietary supplement. | Pharmatech LLC | Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia. | Class II |
| 2016-11-02 | Pedia D-Vite Drops, 50 mL, OTC Non-Sterile. Dietary supplement. | Pharmatech LLC | Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia. | Class II |
| 2016-11-02 | Tri-Vitamin, 50 mL, OTC Non-Sterile. Dietary supplement. | Pharmatech LLC | Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia. | Class II |
| 2015-06-17 | Rugby Poly Vitamin Liquid with Iron, 50 ml | Pharmatech Llc | Packaging label does not match individual product labeling. Outside packaging may have incorrect Lot/Exp and product identity. | Class II |
| 2015-06-17 | Rugby Poly Vitamin Liquid, 50ml | Pharmatech Llc | Packaging label does not match individual product labeling. Outside packaging may have incorrect Lot/Exp and product identity. | Class II |
Questions
- How many FDA recalls has Pharmatech LLC had?
- The FDA has published 42 food recall enforcement records naming Pharmatech LLC between 2015 and 2018. Those records cover 3 separate recall events: the agency opens one record per product code, so one recall of a product line appears as many records.
- Does a high recall count mean a firm is unsafe?
- Not on its own. Most FDA food recalls are initiated voluntarily by the firm, and a recall is the firm removing product from the market, which is what a working food safety plan is supposed to produce. Record counts also scale with the number of product codes a firm carries rather than with the number of things that went wrong.
A recall is the end of an evidence trail that either existed or did not. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.
Early accessRecall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.