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. 2,877 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,877 in last 12 months

Showing 57815800 of 55,713 recalls

Medical DeviceJune 11, 2024· Merit Medical Systems, Inc.

Recalled Item: Various Merit Medical convenience kits that contain recalled Jiangsu Shenli...

The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2024· Merit Medical Systems, Inc.

Recalled Item: Various Merit Medical convenience kits that contain recalled Jiangsu Shenli...

The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2024· Merit Medical Systems, Inc.

Recalled Item: Various Merit Medical convenience kits that contain recalled Jiangsu Shenli...

The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2024· Merit Medical Systems, Inc.

Recalled Item: Various Merit Medical convenience kits that contain recalled Jiangsu Shenli...

The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2024· Merit Medical Systems, Inc.

Recalled Item: Various Merit Medical convenience kits that contain recalled Jiangsu Shenli...

The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2024· Merit Medical Systems, Inc.

Recalled Item: Various Merit Medical convenience kits that contain recalled Jiangsu Shenli...

The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2024· Merit Medical Systems, Inc.

Recalled Item: Various Merit Medical convenience kits that contain recalled Jiangsu Shenli...

The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2024· Merit Medical Systems, Inc.

Recalled Item: Various Merit Medical convenience kits that contain recalled Jiangsu Shenli...

The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2024· Merit Medical Systems, Inc.

Recalled Item: Various Merit Medical convenience kits that contain recalled Jiangsu Shenli...

The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2024· Canadian Hospital Specialties Ltd.

Recalled Item: Product Name: HIGH FLOW INSUFFLATION TUBING (with Filter) Model/Catalog...

The Issue: A customer found product with incomplete seals of P/N 20400161S, lot #185198...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2024· Ethicon Sarl, a Johnson & Johnson Company

Recalled Item: SURGICEL FIBRILLAR 1INX2IN(2.5CMX5.1CM) Recalled by Ethicon Sarl, a Johnson...

The Issue: Some foil pouches were found torn open, impacting the sterile barrier which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2024· Ethicon Sarl, a Johnson & Johnson Company

Recalled Item: SURGICEL FIBRILLAR 1INX2IN(2.5CMX5.1CM) Recalled by Ethicon Sarl, a Johnson...

The Issue: Some foil pouches were found torn open, impacting the sterile barrier which...

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

Class II — Potential Health HazardOngoing
DrugJune 10, 2024· Brands International Corporation

Recalled Item: Oatmeal Daily Moisturizing Body Lotion (1.3% Dimethicone) Recalled by Brands...

The Issue: Microbial Contamination of Non-Sterile Products: confirmed presence of mold...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 10, 2024· BioFire Diagnostics, LLC

Recalled Item: BIOFIRE FILMARRAY Pneumonia Panel plus Recalled by BioFire Diagnostics, LLC...

The Issue: Pneumonia panels have an increased risk of control failures due to an issue...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2024· BioFire Diagnostics, LLC

Recalled Item: BIOFIRE FILMARRAY Pneumonia Panel Recalled by BioFire Diagnostics, LLC Due...

The Issue: Pneumonia panels have an increased risk of control failures due to an issue...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2024· Randox Laboratories Ltd.

Recalled Item: RX Series CYSC- Cystatin C Reagent -Intended for in vitro Recalled by Randox...

The Issue: Cystatin C Reagent marketed without a 510 (k)

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2024· Rygel Advanced Machines d/b/a Omtech Laser

Recalled Item: OMTech Desktop Laser Engraver Recalled by Rygel Advanced Machines d/b/a...

The Issue: Lack of redundant interlocks, missing required labels and certification...

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

Class II — Potential Health HazardOngoing
DrugJune 5, 2024· Homeocare Laboratories, Inc.

Recalled Item: STELLALIFE ADVANCED FORMULA Peppermint Recalled by Homeocare Laboratories,...

The Issue: Microbial Contamination of Non-Sterile Products: presence of Terribacillus...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2024· Homeocare Laboratories, Inc.

Recalled Item: STELLALIFE VEGA Oral Care Recalled by Homeocare Laboratories, Inc. Due to...

The Issue: Microbial Contamination of Non-Sterile Products: multiple Bacillus species...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 5, 2024· Beckman Coulter Mishima K.K.

Recalled Item: DxC 500 AU Clinical Chemistry Analyzer Recalled by Beckman Coulter Mishima...

The Issue: There are two software bug issues with the analyzer. Issue 1: When a...

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

Class II — Potential Health HazardOngoing