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. 2,504 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,504 in last 12 months

Showing 2406124080 of 52,000 recalls

DrugFebruary 6, 2019· Ecolab Inc

Recalled Item: Moisturizing Gel Hand Sanitizer (Ethyl Alcohol 62%) Recalled by Ecolab Inc...

The Issue: Chemical Contamination: low levels of various substituted benzene (aromatic)...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 6, 2019· Ecolab Inc

Recalled Item: Advanced Gel Hand Sanitizer (Ethyl alcohol 62%) Recalled by Ecolab Inc Due...

The Issue: Chemical Contamination: low levels of various substituted benzene (aromatic)...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 5, 2019· Abbott Ireland Diagnostics Division

Recalled Item: Abbott ARCHITECT Estradiol Reagent Kit - Product Usage: The ARCHITECT...

The Issue: Patient results may be falsely elevated. This patient impact only applies to...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2019· Abbott Ireland Diagnostics Division

Recalled Item: Abbott Alinity i Estradiol Reagent Kit - Product Usage: Alinity Recalled by...

The Issue: Patient results may be falsely elevated. This patient impact only applies to...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2019· CP Medical Inc

Recalled Item: Plain and Chromic Gut Absorbable Surgical Sutures Recalled by CP Medical Inc...

The Issue: Potential compromise of product sterility after routine monitoring for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2019· US Endoscopy Group Inc

Recalled Item: US Endoscopy Padlock Clip defect closure system The Recalled by US Endoscopy...

The Issue: Potential esophageal laceration during a patient procedure

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2019· Roche Diagnostics Corporation

Recalled Item: Cobas¿ infinity central lab IT solution Material Number: 07154003001...

The Issue: Using the following versions of cobas infinity software (2.0 thorough 2.5),...

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

Class II — Potential Health HazardOngoing
DrugFebruary 4, 2019· ICU Medical Inc

Recalled Item: 0.9% Sodium Chloride Injection Recalled by ICU Medical Inc Due to CGMP...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 4, 2019· Akorn Inc

Recalled Item: Moisturizing Lubricant Eye Drops Recalled by Akorn Inc Due to Failed...

The Issue: Failed Stability Specification: out of specification results for Sodium...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 4, 2019· Encore Medical, Lp

Recalled Item: EMPOWR Locking Femoral Impactor Recalled by Encore Medical, Lp Due to The...

The Issue: The firm has received reports/complaints concerning the breakage of the tips...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2019· Cook Inc.

Recalled Item: Cook Transseptal Needle Recalled by Cook Inc. Due to The products were...

The Issue: The products were manufactured without a back bevel on the needle tip. This...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 1, 2019· Zimmer Trabecular Metal Technology, Inc.

Recalled Item: NexGenTrabecular Metal Tibial Half Block Augment Recalled by Zimmer...

The Issue: Potentially comingled, resulting in the product in the box potentially not...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2019· Zimmer Trabecular Metal Technology, Inc.

Recalled Item: NexGenTrabecular Metal Tibial Half Block Augment Recalled by Zimmer...

The Issue: Potentially comingled, resulting in the product in the box potentially not...

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

Class II — Potential Health HazardOngoing
DrugFebruary 1, 2019· Mylan Institutional Inc

Recalled Item: Levoleucovorin Injection Recalled by Mylan Institutional Inc Due to Presence...

The Issue: Presence of Particulate Matter: particulate matter identified as copper salts

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 1, 2019· Mylan Pharmaceuticals Inc.

Recalled Item: Dymista (azelastine hydrochloride and fluticasone propionate) Nasal Spray...

The Issue: Defective Container: Potential for broken glass in the neck area of the...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 31, 2019· Dr. Reddy's Laboratories, Inc.

Recalled Item: Divalproex Sodium Extended-release Tablets Recalled by Dr. Reddy's...

The Issue: Failed Dissolution Specifications: Out of specification results observed for...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 31, 2019· Medline Industries Inc

Recalled Item: Semi-Rigid Suction Canister Recalled by Medline Industries Inc Due to...

The Issue: Potential for the Semi-Rigid canister lid to fragment during use.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2019· Microbiologics Inc

Recalled Item: Cepheid Respiratory Control Panel Catalog #8199 for in vitro diagnostic use...

The Issue: Cepheid Xpert Respiratory Control Panel (Catalog #8199) has an reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2019· Matrix Surgical Holdings, LLC

Recalled Item: OMNIPORE Surgical Implant Petite Paranasal - Right - Product Usage: Recalled...

The Issue: Product mislabeling.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2019· Matrix Surgical Holdings, LLC

Recalled Item: OMNIPORE Surgical Implant Petite Paranasal - Left - Product Usage: Recalled...

The Issue: Product mislabeling.

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

Class II — Potential Health HazardOngoing