Product Recalls in Tennessee
Product recalls affecting Tennessee — including food, drugs, consumer products, medical devices, and vehicles distributed to Tennessee. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,452 recalls have been distributed to Tennessee in the last 12 months.
Showing 35781–35800 of 52,000 recalls
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: 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 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: American Surgical Ray-Cot 1" x 1" : 60-12 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 Delicot 4 mm x 50 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 Ultracot 30 mm x 70 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 Uniqcot 1/2" x 3" : 67-09 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 Tonsil Sponges 1" Large : 50-01 Product Recalled by...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mass Eye & Ear Finger Cot Nasal 2's : Recalled by American Surgical Company...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ellipse ICD (Implantable Cardioverter Defibrillator) Model CD2411-36Q...
The Issue: St. Jude Medical is recalling the Ellipse ICD (Implantable Cardioverter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Trucount Absolute Counting Tubes: Model number: 340334 IVD Recalled by...
The Issue: One lot of lot of BD Trucount tubes may contain tubes from another lot....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X-Ray Diagnostic Table Recalled by Shimadzu Medical Systems Due to Report of...
The Issue: Report of unintentional movement of table to reverse tilting.
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: ALFALFA SEED Recalled by International Sprout Holding Inc. Due to Potential...
The Issue: One sample taken were positive for Salmonella Poly B
Recommended Action: Do not consume. Return to store for a refund or discard.
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: 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: 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.