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. 2,645 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,645 in last 12 months

Showing 1336113380 of 29,188 recalls

Medical DeviceAugust 21, 2019· Zimmer Biomet, Inc.

Recalled Item: Compress Recalled by Zimmer Biomet, Inc. Due to Elevated levels of bacterial...

The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2019· Zimmer Biomet, Inc.

Recalled Item: Copeland HA Resurfacing Head Recalled by Zimmer Biomet, Inc. Due to Elevated...

The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2019· Zimmer Biomet, Inc.

Recalled Item: 2.0MM BALL NOSE GUIDE WIRE Recalled by Zimmer Biomet, Inc. Due to Elevated...

The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2019· Zimmer Biomet, Inc.

Recalled Item: Comprehensive HHR Tess Cleat Recalled by Zimmer Biomet, Inc. Due to Elevated...

The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2019· Zimmer Biomet, Inc.

Recalled Item: GUIDE WIRE 2.2MM X 28IN Recalled by Zimmer Biomet, Inc. Due to Elevated...

The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2019· AZIYO BIOLOGICS

Recalled Item: BioEnvelope Recalled by AZIYO BIOLOGICS Due to Possible suture brittleness...

The Issue: Possible suture brittleness or breakage along the Envelope seam before the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2019· AZIYO BIOLOGICS

Recalled Item: CanGaroo Envelopes labeled as the following: 1. CanGaroo Envelope (Large)...

The Issue: Possible suture brittleness or breakage along the Envelope seam before the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2019· Zimmer GmbH

Recalled Item: Sidus Stem-Free Shoulder Humeral Head 50-18 Item number: 01.04555.500...

The Issue: Incorrect labeling on the products package. The label on the package shows...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2019· Boston Scientific Corporation

Recalled Item: Subcutaneous Implantable Cardioverter Defibrillator (S-ICD) System Recalled...

The Issue: Potential need for device replacement - Elective Replacement Indicator (ERI)...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2019· Boston Scientific Corporation

Recalled Item: Subcutaneous Implantable Cardioverter Defibrillator (S-ICD) System Recalled...

The Issue: Potential need for device replacement - Elective Replacement Indicator (ERI)...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 20, 2019· Repro-Med Systems, Inc.

Recalled Item: 20" 2-Needle 26-Gauge 6mm HlgH-Flo Subcutaneous Safety Needle Sets" Product...

The Issue: Mislabeled needle lengths

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· Intuitive Surgical, Inc.

Recalled Item: da Vinci SP Camera Recalled by Intuitive Surgical, Inc. Due to Some cameras...

The Issue: Some cameras were found to have residual soil adhered to the tip of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· RESPIRATORY THERAPEUTICS GROUP LLC

Recalled Item: RespVent Closed Suction System T-Piece Tracheostomy Adult Recalled by...

The Issue: It has been determined that some units of catheters were not tightly...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· OrthoPediatrics Corp

Recalled Item: Model No. 01-1503-0032 (Adolescent Nail Attachment Bolt). Component of the...

The Issue: Binding can occur between the attachment bolt and intramedullary nail, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· OrthoPediatrics Corp

Recalled Item: Model No. 01-1501-0032 (Child Nail Attachment Bolt). Component of the...

The Issue: Binding can occur between the attachment bolt and intramedullary nail, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· OrthoPediatrics Corp

Recalled Item: OrthoPediatrics Adolescent attachment bolt used with the Pediatric Nailing...

The Issue: Interference can occur between the adolescent attachment bolt and the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...

The Issue: Flow cytometers, when used with specific tubes may experience excessive...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...

The Issue: Flow cytometers, when used with specific tubes may experience excessive...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...

The Issue: Flow cytometers, when used with specific tubes may experience excessive...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...

The Issue: Flow cytometers, when used with specific tubes may experience excessive...

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

Class II — Potential Health HazardOngoing