Teligent Pharma, Inc. recalls Triamcinolone Acetonide Ointment USP, 0.5%, Net Wt. 15 grams tube, Rx Only, Teligent Pharma, Inc., Buena, New Jersey 08310, NDC…
cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
Read the official notice →- Date
- 2022-03-30
- Country
- United States
- Brand
- Teligent Pharma
- Product
- Triamcinolone Acetonide Ointment USP, 0.5%, Net Wt. 15 grams tube, Rx Only, Teligent Pharma, Inc., Buena, New Jersey 08310, NDC…
- Classification
- Class II
- Units
- Nationwide in the USA and Puerto Rico
- Category
- Drugs & medical
- Source
- FDA · Drug
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More Teligent Pharma recalls
- 2022-02-23
US
Teligent Pharma, Inc. recalls Erythromycin Topical Gel USP, 2%, Net Wt 30 g tube, Rx only, Manufactured by: Teligent Pharma, Inc., Buena, NJ 08310, Distributed by:…
Failed Impurities/Degradation Specifications: Lot not meeting specification for Unknown Max Related Compounds.
- 2022-01-05
US
Teligent Pharma, Inc. recalls Betamethasone Dipropionate Lotion USP, 0.05% (Augmented), 30 mL bottle, (29 g), Rx Only, Teligent Pharma Inc., Buena, NJ, 08310, NDC…
Failed Stability Specifications: lot did not meet specification for the Active Pharmaceutical Ingredient (API) particle test, which was determined through routine stability testing
US
Teligent Pharma, Inc. recalls Lidocaine Hydrochloride, Topical Solution USP, 4% (40 mg/mL), packaged in 50 mL screw cap bottles, Rx Only, Manufactured by Teligent…
Superpotent Drug: Minimally superpotent
FDA · DrugTeligent Pharma, Inc.Distributed to a wholesaler in CO who further distributed Nationwide in the USAOfficial notice →US
Teligent Pharma, Inc. recalls Lidocaine Hydrochloride, Topical Solution USP, 4% (40 mg/mL), packaged in 50 mL screw cap bottles, Rx Only, Manufactured by Teligent…
Superpotent Drug
FDA · DrugTeligent Pharma, Inc.Distributed to a wholesaler in CO who further distributed Nationwide in the USAOfficial notice →- 2021-12-22
US
Teligent Pharma, Inc. recalls Lidocaine Hydrochloride Topical Solution USP 4% (40 mg/mL), 50 mL glass bottles, Rx Only, Teligent Pharma Inc., Buena, NJ 08310, NDC…
CGMP Deviations: Lots recalled because they were manufactured at the same facility using the same components as the products that had cracked seals in caps that were found to be superpotent.
US
Other drugs & medical recalls in the United States
- 2022-03-30
US
Rock Town Distillery, Inc. recalls ROCK TOWN - DISTILLERY - HAND SANITIZER, Alcohol Antiseptic 70%, Topical Solution packaged in a) 375 mL (12.7 fl. oz.), NDC…
CGMP Deviations: FDA analysis found product to contain acetal and acetaldehyde above specification limits.
US
Direct Rx recalls Diclofenac Sodium Topical Solution 1.5%, 150 mL, Rx only, Packaged and Distributed by: Direct Rx Dawsonville, GA 30534 Mfg. For SOLA…
Defective Container: Leaking containers.
US
US
Blaine Labs Inc recalls REVITADERM WOUND CARE GEL, (Benzalkonium Chloride in a gel containing transforming growth factor-b), 0.1%, packaged in 29.6 mL (1.0 FL OZ)…
Microbial Contamination of Non-sterile Product; FDA analysis found the product to be contaminated with Bacillus cereus.
- 2022-03-23
US
GE Healthcare, LLC recalls GE Healthcare CARESCAPE Central Station (CSCS) V2.0x MAI700 (Integrated), REF 2082278-001, and MAS700 (Desktop, REF 2082279-001.
If the CARESCAPE Central Station v2.0 is used with an unapproved keyboard, the audio can be muted resulting in loss of audible alarms.
FDA · DeviceGE Healthcare, LLCWorldwide distribution - US nationwide, including Puerto Rico. There was also…Official notice →US
Bio-Rad Laboratories, Inc. recalls BioPlex 2200 REF 12000650 SYPH T PACK Syphilis Total & RPR Reagent Pack
Due to current concerns related to COVID-19 vaccine interference with the RPR portion of the BioPlex 2200 Syphilis Total & RPR panel, as well as intermittent manufacturing challenges to produce RPR reagents that…
FDA · DeviceBio-Rad Laboratories, Inc.Worldwide distribution U.S. Nationwide distribution in the states of AK, AL,…Official notice →