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. 2,504 recalls have been distributed to Tennessee in the last 12 months.
Showing 26781–26800 of 29,188 recalls
Recalled Item: RigiflexTM 11 Single-Use Achalasia Balloon Dilator Recalled by Boston...
The Issue: Product labeled with incorrect expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...
The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alair Bronchial Thermoplasty Catheter Recalled by Boston Scientific...
The Issue: Boston Scientific has discovered an inconsistent "Use By" expiration date on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SYNCHRON System(s) Lactate (LACT) Reagent. Product Usage: Lactate (LACT)...
The Issue: Beckman Coulter has confirmed customer reports of LACT Lot M210077 failing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAR S4 with Variable Spot Scanning Excimer System (STAR S4) Recalled by...
The Issue: Under specific conditions, there is an unlikely potential to result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...
The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAR S4 IR Excimer System (STAR S4 IR) Mfg by AMO Manufacturing USA Recalled...
The Issue: Under specific conditions, there is an unlikely potential to result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VenaFlow Elite 30B-B and 30BI-B Product Usage: The VenaFlow Elite Recalled...
The Issue: DJO, LLC has recently identified a product safety issue with the battery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: All Elekta digital accelerators with electrons and beam modulator Recalled...
The Issue: Customers are resetting the default values outside recommended factory settings.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SL & SLi Series (Mod 15/18/20/25) Linear Accelerator Used for Recalled by...
The Issue: Customers are resetting the default values outside recommended factory settings.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMICUS Exchange Kit Recalled by Fenwal Inc Due to Fenwal has initiated a...
The Issue: Fenwal has initiated a voluntary Urgent Product Recall for lot FA12C07070 of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIA Medical Collection Bag Recalled by International Biomedical, Ltd. Due to...
The Issue: International Biomedical has received reports of interference between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius Service Replacement 0-Ring. Used in as a service part Recalled by...
The Issue: Incorrect rubber nitrile O-rings distributed instead of the correct material...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S-LIFT Inserter Outer Sleeve Product Usage: The Inserter Sleeve is Recalled...
The Issue: The outer sleeve would not fit over the S-LIFT Inserter assembly because the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GYRUS ACMI Recalled by Gyrus Acmi, Incorporated Due to lack of sterility...
The Issue: lack of sterility assurance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BC Hammock Mesh Sling (Medium) Recalled by Prism Medical Services USA Due to...
The Issue: The product does not meet the firm's size standards, the product was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Instruments 0400-820-000S3 T4 Toga w/Inside Shoulder Ties Recalled...
The Issue: Based on an accelerated aging test for this product packaging, there is an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Instruments 0400-850-000S2 T4 Toga Recalled by Stryker Instruments...
The Issue: Based on an accelerated aging test for this product packaging, there is an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Instruments 0400-710-000 T4 Pullover Toga (S/M) Sterile Recalled by...
The Issue: Based on an accelerated aging test for this product packaging, there is an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Instruments0400-750-000 T4 Toga Recalled by Stryker Instruments Div....
The Issue: Based on an accelerated aging test for this product packaging, there is an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.