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. 2,884 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,884 in last 12 months

Showing 45214540 of 55,713 recalls

Medical DeviceOctober 9, 2024· Shimadzu Corp. Analytical & Measuring Instruments Div.

Recalled Item: Autosampler Recalled by Shimadzu Corp. Analytical & Measuring Instruments...

The Issue: There have been cases of failure of the main board due to condensation water...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE convenience kits labeled as: 1) ORTHO LAMINECTOMY-LF Recalled by...

The Issue: Medline is recalling medical convenience manufactured using certain lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE convenience kits labeled as: 1) BREAST BIOPSY PACK-LF Recalled by...

The Issue: Medline is recalling medical convenience manufactured using certain lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2024· Shimadzu Corp. Analytical & Measuring Instruments Div.

Recalled Item: Autosampler Recalled by Shimadzu Corp. Analytical & Measuring Instruments...

The Issue: There have been cases of failure of the main board due to condensation water...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE convenience kits labeled as: 1) GENERAL ENDOSCOPY PACK Recalled by...

The Issue: Medline is recalling medical convenience manufactured using certain lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2024· Cook Incorporated

Recalled Item: Approach Hydro ST Micro Wire Guide Recalled by Cook Incorporated Due to...

The Issue: Affected device lots have labels that state the incorrect expiration dates.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2024· ETHICON, INC.

Recalled Item: MONOCRYL" (poliglecaprone 25) Suture MONOCRYL" Sutures are indicated...

The Issue: Due a component mix-up in manufacturing, the affected products may contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2024· Cook Incorporated

Recalled Item: Approach CTO Micro Wire Guide Recalled by Cook Incorporated Due to Affected...

The Issue: Affected device lots have labels that state the incorrect expiration dates.

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

Class II — Potential Health HazardOngoing
DrugOctober 8, 2024· C & A Naturistics

Recalled Item: AK Forte Ortiga y Omega 3 Cont. Neto 100 Tabletas Recalled by C & A...

The Issue: Marketed without an Approved NDA/ANDA: FDA analysis found the product to be...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 7, 2024· Nestle Product Technology Center - Nestle Health Science

Recalled Item: Douglas Labs Stress-B-Plus Dietary Supplement Recalled by Nestle Product...

The Issue: Nestle Health Science (NHS U.S., LLC) is initiating a recall of Douglas Labs...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 7, 2024· DRG International, Inc.

Recalled Item: DRG:HYBRiD-XL Insulin. Model/Catalog Number: HYE-5361 Recalled by DRG...

The Issue: The user of the assay may either face a failure message during...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2024· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Zenition 70 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...

The Issue: Potential for the Mains Control Unit board fuse may blow out during system...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2024· Philips Respironics, Inc.

Recalled Item: Trilogy Evo Universal Ventilator. Model Number DS2000X11B. Intended for...

The Issue: Potential for in-line nebulizer configuration in certain locations to result...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 7, 2024· Philips Respironics, Inc.

Recalled Item: Aeris EVO. Model Number: VT2110X24B. Intended for invasive and non-invasive...

The Issue: Potential for in-line nebulizer configuration in certain locations to result...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 7, 2024· Philips Respironics, Inc.

Recalled Item: Trilogy Evo O2. Model Numbers: FP2100X10 Recalled by Philips Respironics,...

The Issue: Potential for in-line nebulizer configuration in certain locations to result...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 7, 2024· Philips Respironics, Inc.

Recalled Item: Trilogy Evo. Model Numbers: DS2110X11B Recalled by Philips Respironics, Inc....

The Issue: Potential for in-line nebulizer configuration in certain locations to result...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 7, 2024· Philips Respironics, Inc.

Recalled Item: Garbin Evo. Model Number: LD2110X23B. Intended for invasive and non-invasive...

The Issue: Potential for in-line nebulizer configuration in certain locations to result...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 7, 2024· Philips Respironics, Inc.

Recalled Item: Trilogy EV300. Model Numbers: DS2200X11B Recalled by Philips Respironics,...

The Issue: Potential for in-line nebulizer configuration in certain locations to result...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 7, 2024· Philips Respironics, Inc.

Recalled Item: LifeVent EVO2. Model Number: SP2100X26B. Intended for invasive and...

The Issue: Potential for in-line nebulizer configuration in certain locations to result...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 7, 2024· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Zenition 50 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...

The Issue: Potential for the Mains Control Unit board fuse may blow out during system...

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

Class II — Potential Health HazardOngoing