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. 1,056 recalls have been distributed to Tennessee in the last 12 months.
Showing 17401–17420 of 52,000 recalls
Recalled Item: OSS Polyethylene Tibial Bushing Recalled by Biomet, Inc. Due to Specific...
The Issue: Specific lots of multiple sterile medical devices may have a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: M/H MODULAR STEM Recalled by Biomet, Inc. Due to Specific lots of multiple...
The Issue: Specific lots of multiple sterile medical devices may have a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titanium IFS Recalled by Biomet, Inc. Due to Specific lots of multiple...
The Issue: Specific lots of multiple sterile medical devices may have a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHOENIX Recalled by Biomet, Inc. Due to Specific lots of multiple sterile...
The Issue: Specific lots of multiple sterile medical devices may have a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RingLoc+ Quick Connect Drill Bit Recalled by Biomet, Inc. Due to Specific...
The Issue: Specific lots of multiple sterile medical devices may have a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RapidFire Clip Recalled by Biomet, Inc. Due to Specific lots of multiple...
The Issue: Specific lots of multiple sterile medical devices may have a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Trac System Thinflap 24 MM Burr Hole Plate Recalled by Biomet, Inc....
The Issue: Specific lots of multiple sterile medical devices may have a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Cancellous Thread Recalled by Biomet, Inc. Due to Specific lots of...
The Issue: Specific lots of multiple sterile medical devices may have a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anagrelide Capsules Recalled by Torrent Pharma Inc Due to Failed Dissolution...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Neostigmine Methylsulfate PF Inj. 5 mg/5 mL Recalled by US Compounding Inc...
The Issue: Labelling: Missing label.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...
The Issue: There is an increased likelihood of the introducer sheath separating at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...
The Issue: There is an increased likelihood of the introducer sheath separating at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...
The Issue: There is an increased likelihood of the introducer sheath separating at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...
The Issue: There is an increased likelihood of the introducer sheath separating at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...
The Issue: There is an increased likelihood of the introducer sheath separating at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...
The Issue: There is an increased likelihood of the introducer sheath separating at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexor Tuohy-Borst Side-Arm Introducer (Shuttle Select) Recalled by Cook...
The Issue: There is an increased likelihood of the introducer sheath separating at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...
The Issue: There is an increased likelihood of the introducer sheath separating at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...
The Issue: There is an increased likelihood of the introducer sheath separating at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...
The Issue: There is an increased likelihood of the introducer sheath separating at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.