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. 1,740 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
1,740 in last 12 months

Showing 4726147280 of 52,000 recalls

Medical DeviceJune 11, 2013· Church & Dwight Inc

Recalled Item: Sodium Bicarbonate Recalled by Church & Dwight Inc Due to Church and Dwight...

The Issue: Church and Dwight Co., Inc. has initiated a recall for Sodium Bicarbonate,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· Integra LifeSciences Corp.

Recalled Item: Inegra Licox Brain Tissue Oxygen Monitoring 1 x Complete Brain Recalled by...

The Issue: Integra LifeSciences Corporation has determined that there is a possibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· GE Healthcare It

Recalled Item: The Centricity PACS Workstation is intended for use as a Recalled by GE...

The Issue: GE has recently become aware of potential issues due to out of context...

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

Class II — Potential Health HazardOngoing
DrugJune 11, 2013· Church & Dwight Inc

Recalled Item: Sodium Bicarbonate Powder Recalled by Church & Dwight Inc Due to Presence of...

The Issue: Presence of Foreign Substance: raw material recalled due to stainless steel...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 11, 2013· Church & Dwight Inc

Recalled Item: Sodium Bicarbonate Powder Recalled by Church & Dwight Inc Due to Presence of...

The Issue: Presence of Foreign Substance: raw material recalled due to stainless steel...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 11, 2013· Church & Dwight Inc

Recalled Item: Sodium Bicarbonate Powder Recalled by Church & Dwight Inc Due to Presence of...

The Issue: Presence of Foreign Substance: raw material recalled due to stainless steel...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 11, 2013· Church & Dwight Inc

Recalled Item: Sodium Bicarbonate Powder Recalled by Church & Dwight Inc Due to Presence of...

The Issue: Presence of Foreign Substance: raw material recalled due to stainless steel...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 11, 2013· Church & Dwight Inc

Recalled Item: Sodium Bicarbonate Powder Recalled by Church & Dwight Inc Due to Presence of...

The Issue: Presence of Foreign Substance: raw material recalled due to stainless steel...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 11, 2013· Bethel Nutritional Consulting, Inc

Recalled Item: Bethel 30 capsules Recalled by Bethel Nutritional Consulting, Inc Due to...

The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found this product...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 10, 2013· Biomet 3i, LLC

Recalled Item: Osseotite Parallel Walled Certain 4mm(D)X 15mm (L) Dental Implant Product...

The Issue: One of the dental implants do not have the internal hex feature. One of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Staar Surgical Co.

Recalled Item: nanoFLEX CC4204A Intraocular Lens Correct aphakia in persons 60 years...

The Issue: STAAR Surgical Company is recalling a limited number of nanoFLEX CC4204A and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Zimmer, Inc.

Recalled Item: Persona (TM) The Personalized Knee System CPS Tibial Articular Surface...

The Issue: Zimmer had received complaints that reported breakage of the Persona Knee...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Steritec Products Mfc. Co., Inc.

Recalled Item: Getinge Assure Accufast BI Test Pack w/ 25 Controls Recalled by Steritec...

The Issue: Mesa Labs, based out of Bozeman, MT, informed SteriTec Products, Inc. of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Steritec Products Mfc. Co., Inc.

Recalled Item: Medline Steam Biological Indicators Recalled by Steritec Products Mfc. Co.,...

The Issue: Mesa Labs, based out of Bozeman, MT, informed SteriTec Products, Inc. of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Steritec Products Mfc. Co., Inc.

Recalled Item: Cardinal BI Stat Biological Test Pack with Instant Readout Integrator...

The Issue: Mesa Labs, based out of Bozeman, MT, informed SteriTec Products, Inc. of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Zimmer, Inc.

Recalled Item: Persona (TM) The Personalized Knee System Tibial Articular Surface...

The Issue: Zimmer had received complaints that reported breakage of the Persona Knee...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Biomet 3i, LLC

Recalled Item: Osseotite 2 Certain Prevail 5mm(D)X 4.1mm (P) X X 11.5mm Recalled by Biomet...

The Issue: One of the dental implants do not have the internal hex feature. One of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Steritec Products Mfc. Co., Inc.

Recalled Item: Medline Med-Checks BI Test packs with Instant Readout Integrator Recalled by...

The Issue: Mesa Labs, based out of Bozeman, MT, informed SteriTec Products, Inc. of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Staar Surgical Co.

Recalled Item: Afinity CQ2015A Intraocular Lens The visual correction of aphakia in...

The Issue: STAAR Surgical Company is recalling a limited number of nanoFLEX CC4204A and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Zimmer, Inc.

Recalled Item: Persona (TM) The Personalized Knee System UC Tibial Articular Surface...

The Issue: Zimmer had received complaints that reported breakage of the Persona Knee...

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

Class II — Potential Health HazardOngoing