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.

52,000 total recalls
2,492 in last 12 months

Showing 2706127080 of 29,188 recalls

Medical DeviceApril 4, 2013· Smith & Nephew, Inc., Endoscopy Div.

Recalled Item: Biosure Driver Recalled by Smith & Nephew, Inc., Endoscopy Div. Due to...

The Issue: Driver does not meet specification, oversized. Driver may not be able to be...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2013· Smith & Nephew, Inc., Endoscopy Div.

Recalled Item: Biosure Ratchet Driver Recalled by Smith & Nephew, Inc., Endoscopy Div. Due...

The Issue: Driver does not meet specification, oversized. Driver may not be able to be...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2013· Remel Inc

Recalled Item: remel RapID Yeast Plus System Recalled by Remel Inc Due to Mislabeling

The Issue: The two reagents supplied in the RapID Yeast Plus System kit (Reagent A and...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2013· B. Braun Medical, Inc.

Recalled Item: 13mm addEASE(TM) Binary Connector with 17 Ga. Needle for use Recalled by B....

The Issue: Possible solution leakage at the interface of the addEASE(TM) Binary...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2013· B. Braun Medical, Inc.

Recalled Item: 20mm addEASE(TM) Binary Connector with 17 Ga. Needle for use Recalled by B....

The Issue: Possible solution leakage at the interface of the addEASE(TM) Binary...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2013· GE Healthcare, LLC

Recalled Item: SOLAR 8000 AND TRANSPORT PRO WITH PATIENT DATA MODULE (Marketed Recalled by...

The Issue: GE Healthcare has recently become aware of a potential safety issue due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...

The Issue: GE Healthcare has recently become aware of a potential safety issue due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...

The Issue: GE Healthcare has recently become aware of a potential safety issue due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2013· Toshiba American Medical Systems Inc

Recalled Item: TOSHIBA Kalare Diagnostic X-Ray System K110785 Recalled by Toshiba American...

The Issue: Firm initiated recall because when radiographic conditions with the small...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS Immunodiagnostic Products CK-MB Calibrators Recalled by...

The Issue: Internal testing demonstrated that opened-reconstituted VITROS CK-MB...

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

Class III — Low RiskOngoing
Medical DeviceApril 2, 2013· Synvasive Technology Inc

Recalled Item: Product is distributed by Zimmer (Warsaw Recalled by Synvasive Technology...

The Issue: Various reciprocating and oscillating saw blades were incorrectly labeled....

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2013· Hospira Inc.

Recalled Item: List No. 14212-28 Recalled by Hospira Inc. Due to It was discovered that...

The Issue: It was discovered that there was a potential for the piercing pin on certain...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2013· Hospira Inc.

Recalled Item: List No. 14207-28 Recalled by Hospira Inc. Due to It was discovered that...

The Issue: It was discovered that there was a potential for the piercing pin on certain...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2013· Roche Molecular Systems, Inc.

Recalled Item: cobas¿ 4800 system z480 instrument. Integrates fully automated total...

The Issue: In rare instances, channel shifted results have been generated with cobas¿...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2013· Hospira Inc.

Recalled Item: List No. 14211-28 Recalled by Hospira Inc. Due to It was discovered that...

The Issue: It was discovered that there was a potential for the piercing pin on certain...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2013· Hospira Inc.

Recalled Item: List No. 14200-28 Recalled by Hospira Inc. Due to It was discovered that...

The Issue: It was discovered that there was a potential for the piercing pin on certain...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products-HCY Reagent packaged in a kit carton. Catalog#...

The Issue: The firm is recalling the specific lot due to lower than expected results.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2013· Hospira Inc.

Recalled Item: List No. 14210-28 Recalled by Hospira Inc. Due to It was discovered that...

The Issue: It was discovered that there was a potential for the piercing pin on certain...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2013· Hospira Inc.

Recalled Item: List No. 14206-28 Recalled by Hospira Inc. Due to It was discovered that...

The Issue: It was discovered that there was a potential for the piercing pin on certain...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2013· Hospira Inc.

Recalled Item: List No. 14217-28 Recalled by Hospira Inc. Due to It was discovered that...

The Issue: It was discovered that there was a potential for the piercing pin on certain...

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

Class I — Serious Health HazardOngoing