Physicians Total Care, Inc.
Complete recall history across all FDA and CPSC categories — 19 total recalls
Physicians Total Care, Inc. appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.
Drug Recalls (19)
FDA drug safety enforcement actions by Physicians Total Care, Inc.
| Date | Product | Reason | Class |
|---|---|---|---|
| Sep 22, 2014 | CEPHALEXIN MONOHYDRATE CAPSULES,USP, 500 mg, 20-count bottle, Rx only, Manufa... | CGMP deviations: Products were manufactured with active pharmaceutical ingred... | Class II |
| Nov 22, 2013 | Carisoprodol IV ( Carisoprodol Tablets USP) 350mg, RX only. Mfd by: Shasun C... | Presence of Foreign Substance; heavy metals (chromium, titanium etc) and inac... | Class II |
| Sep 11, 2013 | Loratadine 24 HR-OTC,10 mg, 30-count bottle, Manufactured by Novartis Consume... | Failed Tablet/Capsule Specifications: Affected lot numbers may contain chippe... | Class III |
| Jun 17, 2013 | Belladonna Alkaloids/PB (Belladonna Alkaloids / Phenobarbital) Tablets Phenob... | Presence of Foriegn Substance:The manufacturer, West-ward Pharmaceutical, rec... | Class II |
| Mar 18, 2013 | Camila 0.35 mg Tablets, 6 cards of 28 pills, Dist. By: Physicians Total Care,... | Failed Impurity/Degradation Specification; an impurity identified as N-Butyl-... | Class III |
| Mar 2, 2013 | Voltaren 1% Gel, 100 gm tube, Rx only, Dist By: Physicians Total Care, Tulsa ... | Labeling: Incorrect or Missing Lot and/or Expiration Date; This recall is bei... | Class III |
| Nov 15, 2012 | Levothyroxine Tablets, USP (levothyroxine sodium), 0.175 mg, 30 count bottles... | Subpotent; 15 month stability (by mfr) | Class II |
| Feb 20, 2012 | PHYSICIANS TOTAL CARE, TETRACYCLINE, 500 mg, 30 CAPSULES, bottle MFG. BY: TEV... | Presence of Foreign Substance(s): There is a potential for foreign particulat... | Class II |
| Feb 20, 2012 | PHYSICIANS TOTAL CARE, TETRACYCLINE, 250 mg, 30 CAPSULES, bottle MFG. BY: TEV... | Presence of Foreign Substance(s): There is a potential for foreign particulat... | Class II |
| Feb 8, 2012 | Lipitor (Atorvastatin calcium); 40 mg, 30 TABLETS, Rx only, Repacked & distri... | Chemical Contamination: Complaints of an uncharacteristic odor identified as ... | Class II |
| Sep 19, 2011 | Arthrotec 75 (diclofenac sodium and misoprostol) tablets, 75 mg/200 mcg, a) 3... | Tablet Separation: The manufacturer of Arthrotec had recalled the lots that w... | Class II |
| May 23, 2011 | Percocet 10/325 mg tablets, 100-count tablets per bottle, Rx only, Dist. By: ... | Presence of Foreign Tablets/Capsules: One bottle of Percocet 10/325 mg was fo... | Class III |
| Apr 8, 2011 | Enjuvia (synthetic conjugated estrogens, B) tablets, 0.3mg, 30-count tablets ... | Subpotent (Single ingredient) drug : This is a sub recall of Teva's Enjuvia d... | Class III |
| Apr 8, 2011 | Enjuvia (synthetic conjugated estrogens, B) tablets, 0.9mg, 30-count tablets ... | Subpotent (Single ingredient) drug : This is a sub recall of Teva's Enjuvia d... | Class III |
| Apr 8, 2011 | Enjuvia (synthetic conjugated estrogens, B) tablets, 0.625 mg, 30-count table... | Subpotent (Single ingredient) drug : This is a sub recall of Teva's Enjuvia d... | Class III |
| Apr 6, 2011 | Metronidazole Tablets, USP, 500 mg, packaged in a) 10-count tablets per bottl... | Failed Tablet/Capsule Specifications: Some tablets had the potential to not c... | Class II |
| Mar 18, 2011 | Methylprednisolone Tablets, USP, 4 mg, 20 tablets per bottle, Repacked & Dist... | Impurities/Degradation Products; Product is being recalled due to the potenti... | Class II |
| Feb 8, 2011 | Plavix 75 mg, 30 count bottle, NDC (54868-4070-0), Rx only, Manufactured by B... | Chemical Contamination: Uncharacteristic moldy odor due to presence of 2,4,6-... | Class III |
| Oct 4, 2010 | Procrit (epoetin alfa) injection, 20000 units/mL, 4 mL vial; Mfg By: Amgen In... | Presence of Particulate Matter: glass delamination | Class II |
Frequently Asked Questions
A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.
Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.
The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.
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