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. 1,076 recalls have been distributed to Tennessee in the last 12 months.
Showing 14141–14160 of 29,188 recalls
Recalled Item: Arrow¿ JACC with Chlorag+ard Technology Product Code: JR 42041 HPHNM...
The Issue: Lidstock states the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrowg+ard Blue Advance JACC Product Code: CDC 41541 JX1A Recalled by Arrow...
The Issue: Lidstock states the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrowg+ard Blue Advance PICC pre loaded with Arrow¿ VPS" Precision Recalled...
The Issue: Lidstock states the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow¿ JACC with Chlorag+ard Technology Product Code: JR 42063 HPHNM...
The Issue: Lidstock states the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrowg+ard Blue Advance JACC Product Code:CDC 42052 JX1A Recalled by Arrow...
The Issue: Lidstock states the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrowg+ard Blue Advance JACC Product Code: JRT 43541 HPHNM Recalled by Arrow...
The Issue: Lidstock states the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow JACC with Chlorag+ard Technology Jugular Axillo subclavian Central...
The Issue: Lidstock states the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrowg+ard Blue Advance JACC Product Code: CDC 42063 JX1A Recalled by Arrow...
The Issue: Lidstock states the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow PICC with Chlorag+ard Technology Product Code: CDA 45041 HPK1A...
The Issue: Lidstock states the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow¿ JACC with Chlorag+ard¿ Technology Jugular Axillosubclavian Central...
The Issue: Lidstock states the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow¿ JACC with Chlorag+ard Technology Product Code:JR 42563 HPHNM Recalled...
The Issue: Lidstock states the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrowg+ard Blue Advance JACC Product Code: CDC 42041 JX1A Recalled by Arrow...
The Issue: Lidstock states the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Connected OR Cart Recalled by Stryker Corporation Due to There is a...
The Issue: There is a potential problem with firm s Connected OR Cart, 120V resulting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cook Salle Intraoperative Pyeloplasty Stent Set PRODUCT/CATALOG NUMBER/GPN:...
The Issue: Kwart RetroInject Stent Set (Multi-Length) and Salle Intraoperative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cook Kwart Retro-Inject Ureteral Stent Set: PRODUCT/CATALOG NUMBER/GPN: 4.7...
The Issue: Kwart RetroInject Stent Set (Multi-Length) and Salle Intraoperative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monarch Recalled by AURIS HEALTH INC Due to Reports of aspirating biopsy...
The Issue: Reports of aspirating biopsy needle breakage
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureSigns VS3 NBP Recalled by Philips North America, LLC Due to System...
The Issue: System software inhibits the monitor and as a result does not measure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureSigns VS3 NBP Temp Recalled by Philips North America, LLC Due to System...
The Issue: System software inhibits the monitor and as a result does not measure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureSigns VS4 Government Bundle Recalled by Philips North America, LLC Due...
The Issue: System software inhibits the monitor and as a result does not measure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureSigns VS3 NBP Recalled by Philips North America, LLC Due to System...
The Issue: System software inhibits the monitor and as a result does not measure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.