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. 2,509 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,509 in last 12 months

Showing 2408124100 of 29,188 recalls

Medical DeviceSeptember 30, 2014· Signal Medical Corporation

Recalled Item: Symmetric Total Knee Femoral Components Product Usage: Symmetric Total Knee...

The Issue: Packaging of a device was compromised

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2014· Smiths Medical ASD, Inc.

Recalled Item: CADD-Solis Medication Safety Software Recalled by Smiths Medical ASD, Inc....

The Issue: Smiths Medical has identified an issue with a single batch (Lot Number...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2014· Merge Healthcare, Inc.

Recalled Item: Merge Healthcare Recalled by Merge Healthcare, Inc. Due to It has been...

The Issue: It has been reported that during use, the SpO2 value displayed on the Hemo...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2014· Integra LifeSciences Corp.

Recalled Item: Integra Selector Kit Sterile single use device A bi-lumen Recalled by...

The Issue: Some specific lots of Selector Tubing may potentially leak irrigation fluid...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2014· Coloplast Manufacturing US, LLC

Recalled Item: Coloplast Conveen Urine Collection Leg Bag Recalled by Coloplast...

The Issue: Coloplast is recalling the Conveen Contour Leg Bag due to potential leakage...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens Calibrator E Recalled by Siemens Healthcare Diagnostics, Inc Due to...

The Issue: Positive bias for Calibrator E lot kits ending in 38 and 39 with the ADVIA...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2014· Amerx Health Care Corp.

Recalled Item: Amerigel Saturated Gauze Dressing Wound management Recalled by Amerx Health...

The Issue: Formulation deviation

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2014· Biomet, Inc.

Recalled Item: Green Mamba Suture Passer. The Biomet Sports Medicine Mamba instruments...

The Issue: An investigation identified that high level friction may exist between the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2014· Amerx Health Care Corp.

Recalled Item: Amerigel Hydrogel Wound Dressing Wound management Recalled by Amerx Health...

The Issue: Formulation deviation

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2014· Amerx Health Care Corp.

Recalled Item: Amerigel Post-op Surgical Kits Wound management Recalled by Amerx Health...

The Issue: Formulation deviation

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2014· Cook Medical Incorporated

Recalled Item: Spirotome" Soft-Tissue Biopsy Needle Set. The Spirotome Biopsy Needle Set...

The Issue: MEDINVENTS, the manufacturer of the Spirotome" Soft-Tissue Biopsy...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2014· Amerx Health Care Corp.

Recalled Item: Amerigel Daily Dressing Packets Wound management Recalled by Amerx Health...

The Issue: Formulation deviation

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2014· Biomet, Inc.

Recalled Item: Black Mamba Suture Passer. The Biomet Sports Medicine Mamba instruments...

The Issue: An investigation identified that high level friction may exist between the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2014· Merit Medical Systems, Inc.

Recalled Item: Merit Maestro Microcatheter Recalled by Merit Medical Systems, Inc. Due to...

The Issue: These microcatheters were packaged with a 2.8 F distal tip, rather than the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2014· Biomet, Inc.

Recalled Item: Mamba Disposable Nitinol Needle. The Biomet Sports Medicine Mamba...

The Issue: An investigation identified that high level friction may exist between the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2014· Teleflex Medical

Recalled Item: Pilling Knife Handles: a) b) c) Recalled by Teleflex Medical Due to The...

The Issue: The knife handles slot depth is out of specification, so blades may not fit...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Spirit Combo insulin infusion pump sold as part of Recalled by...

The Issue: The insulin pump may lose time and date settings during a power interruption...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2014· Bausch & Lomb Inc- Greenville Solutions Plant

Recalled Item: Equate Moisture Last Multi-Purpose Solution Recalled by Bausch & Lomb Inc-...

The Issue: Product lot did not meet the specification for its disinfectants at the time...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2014· Siemens Healthcare Diagnostics, Inc.

Recalled Item: siemens Dimension¿ Phenytoin Flex¿ Reagent Cartridge The PTN method used...

The Issue: Internal testing has confirmed a low absorbance range between the levels 1...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2014· Joerns Healthcare

Recalled Item: Joerns EasyCare Bed Product Usage: The AC-powered adjustable hospital bed...

The Issue: The Easy-Care Care-Lock feature installed at the foot of the bed may...

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

Class II — Potential Health HazardOngoing