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. 2,585 recalls have been distributed to Texas in the last 12 months.
Showing 46441–46460 of 55,713 recalls
Recalled Item: Laceration Trays Recalled by Medical Action Industries Inc Due to Some of...
The Issue: Some of the sterile kits may have incomplete seals which might compromise...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laceration Kit: W/Needles Recalled by Medical Action Industries Inc Due to...
The Issue: Some of the sterile kits may have incomplete seals which might compromise...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Port-A-Cath Tray Recalled by Medical Action Industries Inc Due to Some of...
The Issue: Some of the sterile kits may have incomplete seals which might compromise...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson Medi-Pak Recalled by Medical Action Industries Inc Due to Some of...
The Issue: Some of the sterile kits may have incomplete seals which might compromise...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mountain House Freeze-Dried Precooked Scrambled Eggs with Ham and Red...
The Issue: Oregon Freeze Dry, Inc. is voluntarily recalling Mountain House Scrambled...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Prosound F75 or F75 The Hitachi Aloka Medical Recalled by Hitachi Aloka...
The Issue: Loosened monitor arm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Nexdrive Micropositioning Drive. Models Ml-1000 and Ml-2000. For...
The Issue: Potential for misalignment of the Z-stage scale. Using one of these devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DATEX-OHMEDA S/5 SINGLE-WIDTH AIRWAY MODULE Recalled by GE Healthcare, LLC...
The Issue: Failure of the CO2 detector in Single-width Airway and Extension modules,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tritium Sternal Plate System Recalled by PIONEER SURGICAL TECHNOLOGY, INC....
The Issue: Lack of Sterility Assurance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra¿ LED Battery Charger Recalled by Integra LifeSciences Corp. Due to...
The Issue: LED battery chargers may prematurely fail and will not charge the LED...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IS4000 da Vinci Xi - Endoscope accessory Recalled by Intuitive Surgical,...
The Issue: In some procedures when using the endoscope in conjunction with the IS4000...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IS4000 da Vinci Xi - Endoscope accessory Recalled by Intuitive Surgical,...
The Issue: In some procedures when using the endoscope in conjunction with the IS4000...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tenor is a mobile passive lift Recalled by ARJOHUNTLEIGH POLSKA SP. ZO.O....
The Issue: ArjoHuntleigh received reports where the Tenor Lift without Scale (spreader...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXACTAMIX 1200 Compounder Recalled by Baxter Healthcare Corp. Due to If the...
The Issue: If the universal ingredient (UI) in an active configuration is changed using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Echinacea Angustifolia Root PE 4: The product is in powder Recalled by...
The Issue: Products contain Azoxystrobin for which no tolerance is allowed per 40 CFR...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Echinacea Agustifolia Root PE 4:1 The product is in powder Recalled by...
The Issue: Products contain Azoxystrobin for which no tolerance is allowed per 40 CFR...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Echinacea Agustifolia PE 4& echinosides The product is in powder Recalled by...
The Issue: Products contain Azoxystrobin for which no tolerance is allowed per 40 CFR...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: MC-500 Multicolor Laser Photocoagulator Recalled by Nidek Inc Due to Laser...
The Issue: Laser aperture label was not affixed to device prior to shipment in the US.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coat-A-Count Direct Androstenedione Recalled by Siemens Healthcare...
The Issue: The assay is demonstrating a higher frequency of results greater than 10...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Attest Auto-reader. Model numbers 390 Recalled by 3M Company - Health...
The Issue: Labeling on units shipped prior to May 16th, 2014 did not contain the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.