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. 2,603 recalls have been distributed to Tennessee in the last 12 months.
Showing 17241–17260 of 29,188 recalls
Recalled Item: NP FEM LT SZ0 NATURAL-KNE NP FEM RT SZ0 NATURAL-KNE Recalled by Zimmer...
The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRCT MIS CR MOB PLT SZ 4 L¿ PRCT MIS Recalled by Zimmer Biomet, Inc. Due to...
The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tapered Screw-Vent MTX Recalled by Zimmer Dental Inc Due to Mislabeling
The Issue: Two lots of the Tapered Screw-Vent Implants, with different outer thread...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEXGEN LPS-FLEX PRECOAT FEMORAL SIZE E-LT This device is indicated Recalled...
The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZIMMER PATELLA FEMORAL JOINT¿ Osteoarthritis Recalled by Zimmer Biomet, Inc....
The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERSYS 10 INCH BEADED FC REV 15.0X250MM BWD LT & Recalled by Zimmer Biomet,...
The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona Partial Knee spacer block instruments Recalled by Zimmer Biomet,...
The Issue: Certain partial knee implant spacer blocks do not fit in the alignment tower...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LPS PRECOAT SRF HDN FEM SZ D-L LPS PRECOAT SRF Recalled by Zimmer Biomet,...
The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CR-FLEX OPT FEM C-R MINUS CR-FLEX OPT FEM D-L MINUS Recalled by Zimmer...
The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CR OPTION FEM COMP SIZE C/L CR OPTION FEM COMP Recalled by Zimmer Biomet,...
The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEXGEN GSF POROUS FEMORAL LPS FLEX SIZE F Recalled by Zimmer Biomet, Inc....
The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: lmmunalysis EDDP Urine Control Set 1 The EDDP Urine Controls Recalled by...
The Issue: The High (125 ng/ml) Control does not meet specification - it has been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syva¿ EMIT¿ 2000 Theophylline Product Usage: The Syva¿ Emit¿ 2000 Recalled...
The Issue: Lot J1 of the Syva¿ EMIT¿ 2000 Theophylline Assay, when run on a Beckman AU...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DERMABOND" PRINEO" Skin Closure System Product Usage: DERMABOND PRINEO...
The Issue: Ethicon discovered that specific lots of DERMABOND"PRINEO"System may not dry...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemotherm¿ Dual Reservoir Cooler/Heater System Models 400CE and 400MR...
The Issue: Due to FDA's safety communication relating to nontuberculous mycobacteria...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apollo Lap-Band AP System Small with RapidPort EZ Product Usage: Recalled by...
The Issue: Component of the Lap-Band system was missing from the package
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Santajoy Ornament & Giftware Co. Recalled by SANTA JOY ORNAMENT & GIFTWARE...
The Issue: It was discovered that the product units it imported may, at peak levels,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rechargeable Li-ion battery used with Puritan Bennett TM 980 Series Recalled...
The Issue: Rechargeable lithium-ion batteries with incorrect firmware that are used in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 15 ML REAGENT CUP Recalled by Horiba Instruments, Inc dba Horiba Medical Due...
The Issue: The ABX PENTRA Reagent Containers do not always sit properly into the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10 ML REAGENT CUP Recalled by Horiba Instruments, Inc dba Horiba Medical Due...
The Issue: The ABX PENTRA Reagent Containers do not always sit properly into the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.