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. 2,492 recalls have been distributed to Tennessee in the last 12 months.
Showing 27521–27540 of 29,188 recalls
Recalled Item: Flexible Grip which is part of the Synthes Universal Nail Recalled by...
The Issue: Synthes is initiating a voluntary recall of the Flexible Grip (Part number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 6Fx90 GUIDING CATH MCV Product Code: GCB60900000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 6Fx90 GUIDING CATH HH Product Code: GHH60900000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 6Fx90 GUIDING CATH S2 Product Code: GSM60900000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Spine 5.2mm Titanium Click ' X Pedicle Screw Dual Recalled by...
The Issue: Lot number 7542279, of the 45 mm Click 'X Pedicle Screw (Part number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Multi-Vector Distractor Body Recalled by Synthes USA HQ, Inc. Due to...
The Issue: It was discovered that the sheer pin on the Multi-Vector Distractor may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Multi-Vector Distractor Recalled by Synthes USA HQ, Inc. Due to It...
The Issue: It was discovered that the sheer pin on the Multi-Vector Distractor may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Large Combination Clamp/Large External Fixation System Recalled by Synthes...
The Issue: The L1 hex nuts, used to tighten the Large Combination Clamp, were oversized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Multi-Vector Distractor - Multi-axial Mandible Distractor (Left)...
The Issue: It was discovered that the sheer pin on the Multi-Vector Distractor may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Oracle Spacer System Slap Hammer Recalled by Synthes USA HQ, Inc....
The Issue: This recall is being initiated in response to complaints received where it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventri Discovery NM 530c Recalled by GE Healthcare, LLC Due to GE Healthcare...
The Issue: GE Healthcare has recently become aware of an incident which caused a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Giraffe OmniBed¿ and Giraffe Incubator p/n 6600-0723-700 (rev A and Recalled...
The Issue: Neonatal beds and incubator display boards may randomly overwrite stored...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns flexible arterial cannula Recalled by Terumo Cardiovascular Systems...
The Issue: Flexible Arterial Cannula and High-Flow Aortic Arch Cannula connectors were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns high-flow aortic arch cannula Recalled by Terumo Cardiovascular...
The Issue: Flexible Arterial Cannula and High-Flow Aortic Arch Cannula connectors were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns high-flow aortic arch cannula Recalled by Terumo Cardiovascular...
The Issue: Flexible Arterial Cannula and High-Flow Aortic Arch Cannula connectors were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns high-flow aortic arch cannula Recalled by Terumo Cardiovascular...
The Issue: Flexible Arterial Cannula and High-Flow Aortic Arch Cannula connectors were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns flexible arterial cannula Recalled by Terumo Cardiovascular Systems...
The Issue: Flexible Arterial Cannula and High-Flow Aortic Arch Cannula connectors were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns flexible arterial cannula Recalled by Terumo Cardiovascular Systems...
The Issue: Flexible Arterial Cannula and High-Flow Aortic Arch Cannula connectors were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LPS Diaphyseal Sleeves Product Usage: The LPS Diaphyseal Sleeves are...
The Issue: DePuy Orthopaedics is initiating a voluntary recall of the LPS Diaphyseal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LPS Diaphyseal Sleeves Product Usage: The LPS Diaphyseal Sleeves are...
The Issue: DePuy Orthopaedics is initiating a voluntary recall of the LPS Diaphyseal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.