Product Recalls in Indiana
Product recalls affecting Indiana — including food, drugs, consumer products, medical devices, and vehicles distributed to Indiana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,012 recalls have been distributed to Indiana in the last 12 months.
Showing 36281–36300 of 53,528 recalls
Recalled Item: American Surgical Policot 1/4" x 1/4" : 90-02 Product Recalled by American...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Surgical Cotton Balls-Non-Strung 1/8" : 31-07 Product Usage:...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Surgical Delicot 13 mm x 60 mm : Recalled by American Surgical...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Surgical Cotton Balls-Strung 3/8" : 30-01 Product Usage: Recalled...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Surgical Ultracot 15 mm x 20 mm : Recalled by American Surgical...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Surgical Americot Blue 3/8" x 3/8" : 20-22S Recalled by American...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mach 4 Mouse Probe vial within the Mach 4 Universal HRP-Polymer Kit Recalled...
The Issue: Biocare Medical has identified a single lot (082715) of its Mach 4 HRP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Surgical Ultracot 30 mm x 90 mm (Glassine) by American Surgical...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Surgical Americot Blue 1/2" x 3" : 20-07S Recalled by American...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Surgical Americot White 1.5 cm x 5.5 cm by American Surgical...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Surgical Americot Blue 1/4" x 1/4" : 20-01S Recalled by American...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Surgical Americot Blue 1/2" x 1" : 20-05S Recalled by American...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fenofibrate Capsules (Micronized) Recalled by Amerisource Health Services...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LGD-Xtreme (ligandrol LGD-4033) Recalled by Invisiblu International LLC Due...
The Issue: Marketed Without An Approved NDA/ANDA: Contains an unapproved drug,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fenofibrate Capsules (Micronized) Recalled by Amerisource Health Services...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: E.cam or Symbia systems that use foresight detectors - Product Recalled by...
The Issue: E. CAM and Symbia system with foresight detectors performing gated or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur CP Immunoassay System Recalled by Siemens Healthcare...
The Issue: The firm identified an issue in sample processing when using EZee-Nest...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pleur-evac Chest Drainage System Recalled by Teleflex Medical Due to The...
The Issue: The label on the Tyvek bag is missing. This is used by customers to identify...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ondansetron Tablets USP Recalled by Dr. Reddy's Laboratories, Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications; 12 month stability time point
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Yogurt Super Soynuts packaged in 16 oz. plastic bags and Recalled by Lee...
The Issue: Product contains undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.