Product Recalls in Texas

Product recalls affecting Texas — including food, drugs, consumer products, medical devices, and vehicles distributed to Texas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,790 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,790 in last 12 months

Showing 1378113800 of 30,921 recalls

Medical DeviceAugust 21, 2019· CTL Medical Corporation

Recalled Item: CEZANNE II TLIF Bullet-Tip Cage Recalled by CTL Medical Corporation Due to...

The Issue: Reports received of the device fracturing during insertion.

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

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

Recalled Item: CEZANNE II TLIF Bullet-Tip Cage Recalled by CTL Medical Corporation Due to...

The Issue: Reports received of the device fracturing during insertion.

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

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

Recalled Item: CEZANNE II TLIF Bullet-Tip Cage Recalled by CTL Medical Corporation Due to...

The Issue: Reports received of the device fracturing during insertion.

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

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

Recalled Item: CEZANNE II TLIF Bullet-Tip Cage Recalled by CTL Medical Corporation Due to...

The Issue: Reports received of the device fracturing during insertion.

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: COMP RVRS Shoulder Baseplates Recalled by Zimmer Biomet, Inc. Due to...

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: BIOMOD PORCOAT HA GLENTRAY 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: BALL NOSE GUIDE WIRE 80CM 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: Various Hip systems Recalled by Zimmer Biomet, Inc. Due to Elevated levels...

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: HA Pins (DFS HA Cort Screw) 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 RS Cleat CAP 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: ACROMIUM FLANGE SET (Custom product) Item No. PM555148 - Product Recalled by...

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: LT DISC ULNA - HA/PC Recalled by Zimmer Biomet, Inc. Due to Elevated levels...

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: HENNESSY LEFT CONST GLENOID HA Recalled by Zimmer Biomet, Inc. Due to...

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: Various Custom Products 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: 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