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 2664126660 of 52,000 recalls

Medical DeviceJune 22, 2018· Clarity Diagnostics Llc

Recalled Item: Clarity Urocheck 10SG Urinalysis Strips Recalled by Clarity Diagnostics Llc...

The Issue: Clarity Diagnostics LLC discovered specific lots of Clarity 10SG Strips are...

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

Class III — Low RiskOngoing
Medical DeviceJune 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Persona Partial Knee System Spacer Block Alignment Tower Recalled by Zimmer...

The Issue: The PPK System Spacer Block Alignment Tower mating feature that mates with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q. angiography system. Model 10848280 Recalled by Siemens Medical...

The Issue: Potential hardware issue which may cause thermal effects and possible damage...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2018· Smiths Medical ASD Inc.

Recalled Item: Aplicare Povidone Iodine Prep Pads packaged within Portex Pro-Vent Arterial...

The Issue: The povidone iodine prep pads packaged with the arterial blood sampling kits...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2018· Smiths Medical ASD Inc.

Recalled Item: Aplicare Povidone Iodine Prep Pads packaged within Portex Pulsator Arterial...

The Issue: The povidone iodine prep pads packaged with the arterial blood sampling kits...

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

Class II — Potential Health HazardOngoing
DrugJune 22, 2018· Akorn, Inc.

Recalled Item: Acetylcysteine for Injection 6 g/30 mL (200 mg/mL). Rx Only. Recalled by...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 22, 2018· Prinova US LLC

Recalled Item: Prinova brand Product - Reginator NV (41825) 25 Kgs Fiber Recalled by...

The Issue: This recall has been identified due to the detection of cyclamates...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodJune 22, 2018· Prinova US LLC

Recalled Item: Amino Life brand Product - L-Leucine Instant Sunflower 25 Kgs Recalled by...

The Issue: This recall has been identified due to the detection of cyclamates...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodJune 22, 2018· Prinova US LLC

Recalled Item: Prinova brand Product - MRI Amintoten Strawberry Powder 25 Kgs Recalled by...

The Issue: This recall has been identified due to the detection of cyclamates...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodJune 22, 2018· Prinova US LLC

Recalled Item: Amino Life brand Product - BCAA 2:1:1 Instant Sunflower 25 Recalled by...

The Issue: This recall has been identified due to the detection of cyclamates...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodJune 22, 2018· Talking Rain Beverage Co Inc

Recalled Item: Sparkling ICE Cherry Limeade Naturally Flavored Sparking Water Recalled by...

The Issue: Sparkling ICE Cherry Limeade, 17 oz. bottles, is recalled after the firm...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 22, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: ARTIS Pheno Model 10849000. Interventional Fluoroscopic X-Ray System Product...

The Issue: Potential hardware issue which may cause thermal effects and possible damage...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Percepta CRT-P MRI SureScan Recalled by Medtronic Inc., Cardiac Rhythm and...

The Issue: Potential for a device reset to occur in Percepta CRT-P MRI SureScan and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Ossur Americas

Recalled Item: Ossur CB Resolve Recalled by Ossur Americas Due to Halo system products...

The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Ossur Americas

Recalled Item: Ossur Recalled by Ossur Americas Due to Halo system products labeled MR...

The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Ossur Americas

Recalled Item: Ossur Skull Pin Recalled by Ossur Americas Due to Halo system products...

The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Baxter Healthcare Corporation

Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6)...

The Issue: The flow rate test verification was not properly executed for certain Sigma...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Johnson & Johnson Surgical Vision Inc

Recalled Item: Abbott TECNIS 1-Piece Aspheric Acrylic IOL with the TECNIS iTEC Recalled by...

The Issue: Expired intraocular lenses were distributed.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Becton Dickinson & Co.

Recalled Item: BD BBL GC-Lect Agar Recalled by Becton Dickinson & Co. Due to A portion of...

The Issue: A portion of this lot was manufactured using Gentamicin instead of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Percepta CRT-P MRI SureScan Recalled by Medtronic Inc., Cardiac Rhythm and...

The Issue: Potential for a device reset to occur in Percepta CRT-P MRI SureScan and...

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

Class II — Potential Health HazardOngoing