Two types of blood pressure medications sold by Lupin Pharmaceuticals Inc
What is being recalled? Irbesartan and Irbesartan HCTZ manufactured by Lupin Pharmaceuticals
What’s being recalled? Irbesartan, 75 mg, 30-count bottles with lot Nos
Article The hypertension medication is again being recalled due to carcinogenic impurities
Consumers can determine which lots have been recalled here
The MHRA today has issued a recall for 31 batches of Irbesartan-containing medicinal products and 2 batches of Losartan-containing medicinal products due to
Two companies have recalled dietary supplements after testing found they contained a poisonous plant
Raw Farm LLC, a producer of raw dairy products that include cheese, butter, and milk, has voluntarily recalled four of its cheddar products in connection to a
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More than 1,321 recalls were issued last year for human drug products that were defective or violated laws enforced by The MHRA today has issued a recall for 31 batches of Irbesartan-containing medicinal products and 2 batches of Losartan-containing medicinal products due to contamination with 5- (4 What’s being recalled? Irbesartan, 75 mg, 30-count bottles with lot Nos
6 million) than either valsartan or losartan, and fewer lots of it have been identified as containing cancer-causing
Bridgewater, NJ, Alembic Pharmaceuticals, Inc is voluntarily recalling one lot of Since then, the number of valsartan products being recalled and has grown, while products containing two other ‘sartans’ used to treat high blood pressure – losartan (losartan potassium hctz) and irbesartan – have also been recalled by the FDA
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Hikma and Westminster are not actively marketing irbesartan tablets
The FDA named three ARBs in the agency's recall updates: valsartan, losartan, and irbesartan
By Christopher Sharp 12:34, Tue, Nov 30 There is yet another recall of blood pressure medications due to unacceptable levels of a substance that may cause cancer
This recall was prompted due to the detection of trace Initial recall notice: Batch Number 0R855 Exp date: Sep 2023 Revised recall notice: Batch Number 0R855 Exp date: Apr 2023 Aprovel 300mg Film-Coated Tablets, EU/1/97/046/027, (PLGB 04425/0789 This recall is for pharmacies and wholesalers, and not at patient-level
Regular Mail or Fax: or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1 Ed October 7, 2022 at 3:38 pm
It’s a drug called an angiotensin receptor blocker (ARB A drug recall is the most effective way to protect the public from a defective or potentially harmful product
The other two are N-Nitrosodimethylamine (NDMA) and N-Nitrosodiethylamine (NDEA)