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. 2,690 recalls have been distributed to Tennessee in the last 12 months.
Showing 4501–4520 of 29,188 recalls
Recalled Item: Ureteral dilator Recalled by Coloplast Manufacturing US, LLC Due to A...
The Issue: A possible sterility issue (e.g. a breach in sterile packaging) was detected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HDS Traction Boot II Recalled by Baxter Healthcare Corporation Due to Baxter...
The Issue: Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Galaxy System (specifically GAL-019 Recalled by Noah Medical Due to Due to a...
The Issue: Due to a misaligned calibration of the wired controller that may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Route 92 Medical Recalled by ROUTE 92 MEDICAL INC Due to Their is the...
The Issue: Their is the potential for distal tip separation at the proximal marker band...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Route 92 Medical Recalled by ROUTE 92 MEDICAL INC Due to Their is the...
The Issue: Their is the potential for distal tip separation at the proximal marker band...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Route 92 Medical Recalled by ROUTE 92 MEDICAL INC Due to Their is the...
The Issue: Their is the potential for distal tip separation at the proximal marker band...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Route 92 Medical Full Length 070 Access System Recalled by ROUTE 92 MEDICAL...
The Issue: Their is the potential for distal tip separation at the proximal marker band...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Route 92 Medical 070 Reperfusion System Recalled by ROUTE 92 MEDICAL INC Due...
The Issue: Their is the potential for distal tip separation at the proximal marker band...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERSEAL 5 mm Recalled by Olympus Corporation of the Americas Due to Upon...
The Issue: Upon initial activation of the seal function, the POWERSEAL non-conformance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERSEAL 5 mm Recalled by Olympus Corporation of the Americas Due to Upon...
The Issue: Upon initial activation of the seal function, the POWERSEAL non-conformance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERSEAL 5 mm Recalled by Olympus Corporation of the Americas Due to Upon...
The Issue: Upon initial activation of the seal function, the POWERSEAL non-conformance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tablo Hemodialysis System Recalled by Outset Medical, Inc. Due to...
The Issue: Hemodialysis System, pre and post dialyzer peroxide-cured silicone tubing,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CryoValve SG Cryopreserved Pulmonary Human Heart Valve Recalled by Artivion,...
The Issue: The blood cultures performed as part of the organ donation process were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KWIK-STIK Rhizopus stolonifer (+) derived from ATCC 6227b Recalled by...
The Issue: The positive control material (Rhizopus stolonifer) within the KWIK-STIK...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exactech Equinoxe GLENOID Recalled by Exactech, Inc. Due to The packaging of...
The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exactech Equinoxe GLENOID Recalled by Exactech, Inc. Due to The packaging of...
The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exactech Equinoxe Constrained Humeral Liner: Item Numbers: a) 320-40-10...
The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exactech Equinoxe REVERSE SHOULDER Recalled by Exactech, Inc. Due to The...
The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exactech Equinoxe Humeral Liner: Item Numbers: a) 320-40-00 Recalled by...
The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exactech Equinoxe CAGE GLENOID Recalled by Exactech, Inc. Due to The...
The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.