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. 1,038 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
1,038 in last 12 months

Showing 38401–38420 of 55,713 recalls

Medical DeviceFebruary 10, 2016· Philips Electronics North America Corporation

Recalled Item: evaluemed Infant Heel Warmer 301-1223 Recalled by Philips Electronics North...

The Issue: eValueMed Infant Heel Warmers and eValueMed Infant Transport Mattresses bear...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2016· Philips Electronics North America Corporation

Recalled Item: eValueMed Infant Transport Mattress 301-1015 Recalled by Philips Electronics...

The Issue: eValueMed Infant Heel Warmers and eValueMed Infant Transport Mattresses bear...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2016· Arrow International, Inc., Division of Teleflex Medical Inc.

Recalled Item: FiberOptix Ultra 8 IAB: 8Fr 40cc Recalled by Arrow International, Inc.,...

The Issue: The sheath body may become separated from the sheath hub. If the separation...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 10, 2016· Focus Diagnostics Inc

Recalled Item: Simplexa Group A Strep Direct (MOL2850) with Direct Amplification Disc...

The Issue: Focus Diagnostics is recalling the Direct Amplification Discs (DAD) supplied...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 10, 2016· Focus Diagnostics Inc

Recalled Item: Simplexa HSV 1&2 Direct (MOL2150) with Direct Amplification Disc (MOL1451...

The Issue: Focus Diagnostics is recalling the Direct Amplification Discs (DAD) supplied...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 10, 2016· Focus Diagnostics Inc

Recalled Item: Simplexa Flu A/B & RSV Direct (MOL2650) with Direct Amplification Disc...

The Issue: Focus Diagnostics is recalling the Direct Amplification Discs (DAD) supplied...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2016· Arrow International, Inc., Division of Teleflex Medical Inc.

Recalled Item: Percutaneous Insertion Tray Recalled by Arrow International, Inc., Division...

The Issue: The sheath body may become separated from the sheath hub. If the separation...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 10, 2016· Arrow International, Inc., Division of Teleflex Medical Inc.

Recalled Item: UltraFlex IAB: 7.5Fr 40cc Recalled by Arrow International, Inc., Division of...

The Issue: The sheath body may become separated from the sheath hub. If the separation...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 10, 2016· Arrow International, Inc., Division of Teleflex Medical Inc.

Recalled Item: UltraFlex IAB: 7.5Fr 30cc Recalled by Arrow International, Inc., Division of...

The Issue: The sheath body may become separated from the sheath hub. If the separation...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 10, 2016· Arrow International, Inc., Division of Teleflex Medical Inc.

Recalled Item: RediGuard IAB: 7Fr 30cc Recalled by Arrow International, Inc., Division of...

The Issue: The sheath body may become separated from the sheath hub. If the separation...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 10, 2016· Arrow International, Inc., Division of Teleflex Medical Inc.

Recalled Item: Ultra 8 IAB: 8Fr 30cc Recalled by Arrow International, Inc., Division of...

The Issue: The sheath body may become separated from the sheath hub. If the separation...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 10, 2016· Arrow International, Inc., Division of Teleflex Medical Inc.

Recalled Item: Ultra 8 IAB: 8Fr 40cc Recalled by Arrow International, Inc., Division of...

The Issue: The sheath body may become separated from the sheath hub. If the separation...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 10, 2016· Arrow International, Inc., Division of Teleflex Medical Inc.

Recalled Item: Percutaneous Insertion Tray Recalled by Arrow International, Inc., Division...

The Issue: The sheath body may become separated from the sheath hub. If the separation...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 10, 2016· Deerfield Imaging

Recalled Item: Intra operative MRI Systems: Neuro II-SE Recalled by Deerfield Imaging Due...

The Issue: Emergency helium venting lines (i.e. quench lines) may not have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension clinical chemistry system Recalled by Siemens Healthcare...

The Issue: Siemens Healthcare Diagnostics has received customer complaints regarding QC...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2016· Bard Peripheral Vascular Inc

Recalled Item: Denali Filter-Jugular/Subclavian Delivery System Product Code: DL900J/DL950J...

The Issue: Bard Peripheral Vascular, Inc. is recalling Denali Filter-Jugular/Subclavian...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2016· Bard Peripheral Vascular Inc

Recalled Item: Denali Filter-Femoral Delivery System Product Code: DL900F/DL950F Recalled...

The Issue: Bard Peripheral Vascular, Inc. is recalling Denali Filter-Jugular/Subclavian...

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

Class II — Potential Health HazardOngoing
FoodFebruary 9, 2016· Urban Oven, LLC

Recalled Item: Urban Oven Artisan-Baked Short Bread Cookies Classic Butter All Natural...

The Issue: Urban Oven, LLC is recalling Urban Oven Butter Cookies, Cocoa Cookies, Pecan...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 9, 2016· Urban Oven, LLC

Recalled Item: Urban Oven Artisan-Baked Short Bread Cookies Lemon Pistachio All Natural...

The Issue: Urban Oven, LLC is recalling Urban Oven Butter Cookies, Cocoa Cookies, Pecan...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 9, 2016· Urban Oven, LLC

Recalled Item: Urban Oven Artisan-Baked Short Bread Cookies Cocoa All Natural NET Recalled...

The Issue: Urban Oven, LLC is recalling Urban Oven Butter Cookies, Cocoa Cookies, Pecan...

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

Class II — Potential Health HazardOngoing
Refund