Amring Pharmaceuticals Inc recalls Lysteda (tranexamic acid) USP Tablets, 650 mg, 30 tablets per bottle, Rx Only, Manufactured for: Amring Pharmaceuticals Inc. Berwyn,…
Failed Impurities/Degradation Specifications: Out of specification results obtained for conductivity.
Read the official notice →- Date
- 2023-06-21
- Country
- United States
- Brand
- Amring Pharmaceuticals Inc
- Product
- Lysteda (tranexamic acid) USP Tablets, 650 mg, 30 tablets per bottle, Rx Only, Manufactured for: Amring Pharmaceuticals Inc. Berwyn, PA…
- Classification
- Class III
- Units
- Nationwide in the USA.
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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.
Other drugs & medical recalls in the United States
- 2023-06-21
US
AVKARE LLC recalls Tranexamic Acid USP Tablets, 650 mg, 30 tablets (3X10) Unit Dose, Rx Only, Manufactured for: AvKARE Pulaski, TN 38478, NDC 50268-772-13
Failed Impurities/Degradation Specifications: Out of specification results obtained for conductivity.
US
Jarman's Midwest Cleaning Systems, Inc. recalls SOFT HANDS Alcohol Antiseptic 80%, Topical Solution, HAND SANITIZER, NON-STERILE SOLUTION, cleanpro SUPPLY, 1 US gallon…
Chemical Contamination: FDA testing found Presence of methanol
US
Jarman's Midwest Cleaning Systems, Inc. recalls Isopropyl Alcohol Antiseptic 75%, Topical Solution, Hand Sanitizer Non-sterile Solution, Volume: 3.785 L, plastic gallon…
CGMP deficiencies: Product manufactured at the same site where FDA testing found Presence of methanol in other products.
- 2023-06-14
US
C.R. Bard Inc recalls HydroSil Go Intermittent Urinary Catheters, Catalog Numbers: a) REF 71808, b) REF 71810, c) REF 71812, d) REF 71814, e) REF 71816, f) REF…
Some catheters had a manufacturing defect where the clear resealing label separating from the product foil pouch, resulting in a possible opening into the product packaging that could impact product sterility.
US
Young Dental Manufacturing I, LLC recalls BencoDental iris 5% NaF varnish, WHITE MINT ITEM # 4323-635; cavity varnish
The Iris 5% Fluoride Varnish White Mint package lot 207540 may contain units of 5% Fluoride Varnish Bubblegum.
FDA · DeviceYoung Dental Manufacturing I, LLCUS distribution to Florida, Nevada, and Pennsylvania.Official notice →US
Abbott Ireland Limited recalls Alinity i Anti-TPO Reagent Kit, List Number 09P3521
Due to a manufacturing fill volume error, Alinity i Anti-TPO Reagent contains a marginally lower fill volume than detailed in the Kit Contents section of the Instructions for Use (IFU).
FDA · DeviceAbbott Ireland LimitedUS Nationwide distribution in the states of CA, CO, FL, GA, IL, KY, LA, MD,…Official notice →