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. 2,905 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,905 in last 12 months

Showing 31213140 of 55,713 recalls

Medical DeviceMarch 5, 2025· Advanced Bionics, LLC

Recalled Item: HiResolution" Bionic Ear System - M Battery Charger Model Number CI-5607...

The Issue: Due to incorrect the battery charger being packaged and distributed. Product...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2025· Tornier S.A.S.

Recalled Item: stryker Blueprint Mixed Reality Coracoid Clamp Recalled by Tornier S.A.S....

The Issue: Stryker identified an elevated complaint rate related to difficulties using...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2025· Tornier S.A.S.

Recalled Item: stryker Blueprint Mixed Reality Glenoid Digitizer Recalled by Tornier S.A.S....

The Issue: Stryker identified an elevated complaint rate related to difficulties using...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2025· Tornier S.A.S.

Recalled Item: stryker Blueprint Mixed Reality Depth Stop Pin Recalled by Tornier S.A.S....

The Issue: Stryker identified an elevated complaint rate related to difficulties using...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2025· Tornier S.A.S.

Recalled Item: stryker Blueprint Mixed Reality Instrument Kit Recalled by Tornier S.A.S....

The Issue: Stryker identified an elevated complaint rate related to difficulties using...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE ReNewal ENT Coblator II PROcise XP Wand Recalled by MEDLINE...

The Issue: Medline ReNewal has identified that the drip chambers of affected devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2025· Tornier S.A.S.

Recalled Item: stryker Blueprint Mixed Reality Box Base Recalled by Tornier S.A.S. Due to...

The Issue: Stryker identified an elevated complaint rate related to difficulties using...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE ReNewal Coblator II ENT Evac 70 Xtra HP Recalled by MEDLINE...

The Issue: Medline ReNewal has identified that the drip chambers of affected devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE ReNewal Coblator II Evac 70 Xtra Plasma Wand Recalled by MEDLINE...

The Issue: Medline ReNewal has identified that the drip chambers of affected devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2025· Tornier S.A.S.

Recalled Item: stryker Blueprint Mixed Reality BP MxR Glenoid Pin Guide PPSU + Stainless...

The Issue: Stryker identified an elevated complaint rate related to difficulties using...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2025· Tornier S.A.S.

Recalled Item: stryker Blueprint Mixed Reality Instrument Check Block Recalled by Tornier...

The Issue: Stryker identified an elevated complaint rate related to difficulties using...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2025· Tornier S.A.S.

Recalled Item: stryker HoloBlueprint Application Recalled by Tornier S.A.S. Due to Stryker...

The Issue: Stryker identified an elevated complaint rate related to difficulties using...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE ReNewal ENT Coblator II PROcise mAx Recalled by MEDLINE INDUSTRIES,...

The Issue: Medline ReNewal has identified that the drip chambers of affected devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2025· Tornier S.A.S.

Recalled Item: stryker Blueprint Mixed Reality Glenoid Box Lid Recalled by Tornier S.A.S....

The Issue: Stryker identified an elevated complaint rate related to difficulties using...

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

Class II — Potential Health HazardOngoing
FoodMarch 4, 2025· Tristar Food Wholesale Co Inc

Recalled Item: BaiWei ShanZhuang Recalled by Tristar Food Wholesale Co Inc Due to Product...

The Issue: Product contains cyclamates

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

Class III — Low RiskOngoing
Refund
DrugMarch 4, 2025· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Gabapentin Capsules Recalled by SUN PHARMACEUTICAL INDUSTRIES INC Due to...

The Issue: Cross Contamination

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

Class III — Low RiskOngoing
Refund
DrugMarch 4, 2025· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Gabapentin Capsules Recalled by SUN PHARMACEUTICAL INDUSTRIES INC Due to...

The Issue: Cross Contamination

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

Class III — Low RiskOngoing
Refund
DrugMarch 4, 2025· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Tolterodine Tartrate Extended-Release Capsules Recalled by The Harvard Drug...

The Issue: Failed Dissolution Specifications: Out of specification results obtained...

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

Class III — Low RiskOngoing
Refund
DrugMarch 4, 2025· Chattem Inc

Recalled Item: Unisom Recalled by Chattem Inc Due to CGMP Deviations: Nitrosamine Drug...

The Issue: CGMP Deviations: Nitrosamine Drug Substance Related Issue impurity above the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 4, 2025· Medtronic MiniMed, Inc.

Recalled Item: InPen smart insulin pen Recalled by Medtronic MiniMed, Inc. Due to Insulin...

The Issue: Insulin pens may have been incorrectly assembled therefore users could...

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

Class II — Potential Health HazardOngoing