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.

52,000 total recalls
2,603 in last 12 months

Showing 1708117100 of 29,188 recalls

Medical DeviceDecember 20, 2017· Nidek Inc.

Recalled Item: AUTO REF/KERATOMETER ARK-1s Recalled by Nidek Inc. Due to There is possibly...

The Issue: There is possibly a difference between the measured dioptric value of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Philips Electronics North America Corporation

Recalled Item: Allura Xper FD and and Xper FD ORT - Philips Recalled by Philips Electronics...

The Issue: Extra monitors, so called 7th or 8th monitor, mounted on the Monitor Ceiling...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Ad-Tech Medical Instrument Corporation

Recalled Item: Disposable Drill Kit which includes two drill bits Recalled by Ad-Tech...

The Issue: There is a possibility that DDK2-2.4-30X Disposable Drill Kits, Lot Number...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Zimmer Biomet, Inc.

Recalled Item: ACE Trochanteric Nail System STER L H TROC NAIL 320X9X125 Recalled by Zimmer...

The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Zimmer Biomet, Inc.

Recalled Item: ACE Trochanteric Nail System ATN LAG SCREW 60MM STERILE ATN Recalled by...

The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Zimmer Biomet, Inc.

Recalled Item: ACE Trochanteric Nail System STER TROC NAIL 180X11X140 STER TROC Recalled by...

The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Zimmer Biomet, Inc.

Recalled Item: ACE Trochanteric Nail System STER TROC LAG SCR 70 MM Recalled by Zimmer...

The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Zimmer Biomet, Inc.

Recalled Item: ACE Trochanteric Nail System STER TROC NAIL 125 DEG X Recalled by Zimmer...

The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Zimmer Biomet, Inc.

Recalled Item: ACE Trochanteric Nail System ACE TROCH NAIL 125 DEG. X Recalled by Zimmer...

The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Zimmer Biomet, Inc.

Recalled Item: ACE Trochanteric Nail System STER TROC NAIL 180X13X140 STER TROC Recalled by...

The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Zimmer Biomet, Inc.

Recalled Item: ACE Trochanteric Nail System STER TROC END CAP STER TROC Recalled by Zimmer...

The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Zimmer Biomet, Inc.

Recalled Item: ACE Trochanteric Nail System TROCH NAIL ST 13X180 125DG STRL Recalled by...

The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2017· Paragon 28, Inc.

Recalled Item: P28 JAWS Nitinol Staple System kits are designed for use in an osteotomy...

The Issue: Missing drill guide as stated in the package.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2017· Ventana Medical Systems Inc

Recalled Item: CINtec PLUS Cytology Kit (CE-IVD) Recalled by Ventana Medical Systems Inc...

The Issue: Increased reports of leaking and sticking reagent dispensers for horseradish...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2017· Ventana Medical Systems Inc

Recalled Item: iView DAB IHC Detection Kit Recalled by Ventana Medical Systems Inc Due to...

The Issue: Increased reports of leaking and sticking reagent dispensers for horseradish...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2017· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Cardiac Resynchronization Therapy Defibrillators (CRT-Ds) Recalled by...

The Issue: Possible prevention of high and low voltage therapy in Medtronic Implantable...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2017· Cook Inc.

Recalled Item: Marrs Laparoscopic GIFT Catheters Recalled by Cook Inc. Due to Certain lots...

The Issue: Certain lots of in vitro fertilization (IVF) products were distributed...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2017· Cook Inc.

Recalled Item: 1. SMS Embryo Transfer Set Recalled by Cook Inc. Due to Certain lots of in...

The Issue: Certain lots of in vitro fertilization (IVF) products were distributed...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2017· Cook Inc.

Recalled Item: Echosight Jansen-Anderson Intratubal Transfer Set Recalled by Cook Inc. Due...

The Issue: Certain lots of in vitro fertilization (IVF) products were distributed...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2017· Ventana Medical Systems Inc

Recalled Item: CINtec PLUS Cytology Kit (Canada/Japan) Recalled by Ventana Medical Systems...

The Issue: Increased reports of leaking and sticking reagent dispensers for horseradish...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing