Macleods Pharma Usa Inc recalls Eszopiclone Tablets, USP 1 mg, packaged in 30-count bottles, Rx Only, Manufactured for: Macleods Pharma USA, Inc., Plainsboro, NJ 08536,…
Shortfill: customer complaints of one to three tablets were reported missing from 30 count bottles.
Read the official notice →- Date
- 2022-07-13
- Country
- United States
- Brand
- Macleods Pharma
- Product
- Eszopiclone Tablets, USP 1 mg, packaged in 30-count bottles, Rx Only, Manufactured for: Macleods Pharma USA, Inc., Plainsboro, NJ 08536,…
- Classification
- Class II
- Units
- Distributed Nationwide 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 Details may be shortened or out of date; the official notice is the authoritative source.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 Macleods Pharma recalls
- 2026-04-01
US
- 2024-05-22
US
MACLEODS PHARMA USA, INC recalls Losartan Potassium and Hydrochlorothiazide Tablets, USP 50mg /12.5 mg, 1000-count bottle, Rx only, Manufactured for: Macleods Pharma…
Presence of foreign substance: plastic-like substance.
- 2023-01-25
US
MACLEODS PHARMA USA, INC recalls Levofloxacin Tablets, USP 500 mg; 50-count bottles, Rx Only, Manufactured for: Macleods Pharma USA, Inc. Princeton, NJ 08540;…
Mismatching of the embossing on the tablets (T7) with the embossing mentioned in the package insert (ML63) in the distributed bottles.
- 2022-07-06
US
Macleods Pharma Usa Inc recalls Losartan potassium & Hydrochlorothiazide Tablets 100 mg/25 mg, 30, 90 & 1000 count NDC # 33342-052-07, NDC #33342-052-10 & NDC #…
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
- 2022-05-11
US
Macleods Pharma Usa Inc recalls Losartan Potassium Tablets, USP, 50 mg, a) 30-count bottles (NDC # 33342-045-07), b) 90-count bottles (NDC # 33342-045-10), c) 1000-count…
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
- 2022-04-13
US
Macleods Pharma Usa Inc recalls Risedronate Sodium Tablets, USP, 5 mg, Rx Only, 30-count bottle, Manufactured for: Macleods Pharma USA, Plainsboro, NJ 08536,…
FAILED CONTENT UNIFORMITY SPECIFICATIONS
Other drugs & medical recalls in the United States
- 2022-07-13
US
Golden State Medical Supply Inc. recalls Enalapril Maleate Tablets, USP; 2.5 mg; 90 tablets, NDC 60429-183-90; manufactured by Taro Pharmaceutical Industries, Ltd.;…
CGMP Deviations
FDA · DrugGolden State Medical Supply Inc.Nationwide in the U.S: PA, MA, OH, TX, IL, ND, HIOfficial notice →US
SUN PHARMACEUTICAL INDUSTRIES INC recalls Testosterone Cypionate Injection, USP, 200mg/ml, Rx Only, One Single-dose vial, Distributed by: Sun Pharmaceutical Industries…
CGMP Deviations: Manufacturing deviations were reported due to an abnormal appearance on parts of machinery.
US
Vi-Jon, LLC recalls CVS Health Magnesium Citrate SALINE LAXATIVE, Oral Solution, 1.745 g, Lemon Flavor, 10 FL OZ (296 mL), Distributed by: CVS Pharmacy, Inc.,…
Microbial Contamination of a Non-Sterile Products: Testing of product onfirmed the presence of Gluconacetobacter Liquefaciens
US
- 2022-07-06
US
Haemonetics Corporation recalls TEG 5000 Functional Fibrinogen Reagent, Item No. 07-034
Due to a shift in the citrated blood reference range for a normal population, the ranges stated in the IFU are changing. If the clinician relies solely on affected results in comparison to the normal donor reference…
US
Skytron, Div. The KMW Group, Inc recalls Product Name: GCX Channel Mounting Accessory Model/Catalog Number: H8-300-40-A
Under certain circumstances, the mounting screws may loosen or pull out from the attachment point on the Ergon 3 boom when the GCX Channel Mounting Accessory was used with the VST clamp as a monitor mount on the boom.
FDA · DeviceSkytron, Div. The KMW Group, IncWorldwide distribution - US Nationwide and the countries of Canada and Japan.Official notice →