Preferred Pharmaceuticals, Inc. recalls Diclofenac Sodium Topical Solution, 1.5% w/w, packaged in 150 mL bottles, Rx only, Mfg: SOLA Pharmaceuticals Preferred…
Defective container: Out of specification for container integrity leading to bottles leaking.
Read the official notice →- Date
- 2021-12-22
- Country
- United States
- Brand
- Preferred Pharmaceuticals
- Product
- Diclofenac Sodium Topical Solution, 1.5% w/w, packaged in 150 mL bottles, Rx only, Mfg: SOLA Pharmaceuticals Preferred Pharmaceuticals,…
- Classification
- Class II
- Units
- Distributed to 5 physician consignees located in the following states: CT, FL,…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 Preferred Pharmaceuticals recalls
- 2022-06-01
US
Preferred Pharmaceuticals, Inc. recalls Losartan Potassium & HCTZ Tablets 50mg/12.5 mg, hydrochlorothiazide USP 12.5, Pkg Size: 90, NDC: 68788-7758-09.
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
- 2022-05-04
US
Preferred Pharmaceuticals, Inc. recalls Losartan Potassium Tab. USP 50mg, Pkg Size: 30, Mfg: Lupin Pharmaceuticals, Inc., Preferred Pharmaceuticals, Inc.
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits.
FDA · DrugPreferred Pharmaceuticals, Inc.Nationwide within the U.S to CA, IN and FL.Official notice →- 2022-04-27
US
Preferred Pharmaceuticals, Inc. recalls Diclofenac Sodium Topical Solution 1.5% w/w, Generic for Pennsaid, 150 ml bottle, Rx Only, Mfg: Sola Pharmaceutical, Preferred…
CGMP Deviations: all products within expiry are being recalled because the manufacturing firm, Teligent Pharma, Inc. is discontinuing its stability study program.
- 2022-04-20
US
Preferred Pharmaceuticals, Inc. recalls Econazole Nitrate Cream, 1%, Generic for Spectazole, 30 gm tube, Rx Only, Preferred Pharmaceuticals, Inc., The Physican's…
CGMP Deviations: all products within expiry are being recalled because the manufacturing firm, Teligent Pharma, Inc.is discontinuing its stability study program.
FDA · DrugPreferred Pharmaceuticals, Inc.Product distributed in California and Florida.Official notice →US
Preferred Pharmaceuticals, Inc. recalls Preferred Pharmaceuticals, Inc. The Physician's Solution., Lansoprazole Delayed-Release Capsules, 15mg, Generic for Prevacid,…
Out of specification results observed in dissolution during long term stability testing.
- 2022-03-09
US
Other drugs & medical recalls in the United States
- 2021-12-22
US
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
- 2021-12-15
US
Philips North America Llc recalls BV Endura with Software Release 2.3- A mobile, diagnostic X-ray image acquisition and viewing system. Model Number: 718075
Instructions for Use do not specify the maximum surface temperature of the X-ray tank (assembly housing the X-ray tube, beam filter & cooling oil) and the image intensifier/detector of the system as required an result…
FDA · DevicePhilips North America LlcWorldwide distribution - US Nationwide and the countries of Afghanistan,…Official notice →US
Argon Medical Devices, Inc recalls SuperCore Biopsy Instrument: REF/Product Description: 701114090/SUPERCORE BIOPSY INSTR 14GA X 9CM; 701114150/SUPERCORE BIOPSY INSTR…
Due to component (housing and plunger) detaching from the semi-automatic biopsy instruments.
FDA · DeviceArgon Medical Devices, IncWorldwide distribution - U.S. Nationwide distribution in the states of AK, AL,…Official notice →US
Covidien Llc recalls Puritan Bennett 980 Series Ventilator, 980X2ESDIEC
Manufacturing assembly error where a capacitor within the ventilator was assembled incorrectly, which may cause the device to become inoperable during use.