More medical news from FDA Recalls
Cook Medical Issues Global Recall Of Beacon Tip Angiographic Catheter Products
FDA Recalls : August 3, 2015, 5:51 am
On July 2, 2015, Cook Medical initiated a lot-specific voluntary recall of 2,239 lots of Beacon Tip Angiographic Catheters. Globally, 95,167 devices are subject to this recall. The products include specific versions and lot numbers of the Torcon NB® Advantage Beacon® Tip Catheters (Catalog Prefix HNBR5.0), Royal Flush® Plus Beacon® Tip High-Flow Catheters (Catalog Prefix HNR4.0), and Slip-Cath® Beacon® Tip Catheters (Catalog Prefix SCBR5.0).
The Kraft Heinz Company Voluntarily Recalls Select Varieties of Kraft Singles Products Due to Potential Choking Hazard
FDA Recalls : August 1, 2015, 9:25 am
The Kraft Heinz Company is voluntarily recalling select code dates and manufacturing codes of Kraft Singles individually-wrapped slices due to the possibility that a thin strip of the individual packaging film may remain adhered to the slice after the wrapper has been removed. If the film sticks to the slice and is not removed, it could potentially cause a choking hazard.
John B. Sanfilippo & Son, Inc. Voluntarily Recalls Fisher Brand 10 Ounce Chopped Walnuts Because of Possible Health Risk
FDA Recalls : July 31, 2015, 11:18 am
John B. Sanfilippo & Son, Inc. (JBSS) announced today that it is voluntarily recalling Fisher brand chopped walnuts packaged in 10 ounce plastic bags because some of these products may be contaminated with Salmonella.
Baxter Initiates Voluntary Nationwide Recall Of One Lot Of Iv Solution Due To The Potential For Leaking Containers, Particulate Matter And Missing Port Protectors
FDA Recalls : July 31, 2015, 9:21 am
DEERFIELD, Ill., July 30, 2015 - Baxter International Inc. announced today it is voluntarily recalling one lot of intravenous (IV) solution to the hospital/user level due to the potential for leaking containers, particulate matter and missing port protectors. Baxter was made aware of these issues through customer complaints.
Unichem Pharmaceuticals (USA), Inc. Issues a Voluntary Nationwide Recall of Hydrochlorothiazide Tablets Due to the Potential Presence of Foreign Tablets
FDA Recalls : July 31, 2015, 5:42 am
Unichem Pharmaceuticals (USA), Inc. (Unichem) is voluntarily recalling one lot of Hydrochlorothiazide Tablets 25 mg 1000-count bottle to the consumer level. This recall has been initiated as a precautionary measure due to the identification of a Clopidogrel tablet found in a bottle of the product.