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. 1,151 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
1,151 in last 12 months

Showing 11601–11620 of 30,921 recalls

Medical DeviceSeptember 9, 2020· Smith & Nephew, Inc.

Recalled Item: TWINFIX 5.0MM AB SUTURE ANCHOR-Absorbable Suture anchors Product Number:...

The Issue: Product packaging improper or incomplete seal of the pouch surrounding the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2020· Smith & Nephew, Inc.

Recalled Item: TWINFIX ULTRA PLLA HA 5.5MM W/ NEEDLES- Absorbable Suture anchor Recalled by...

The Issue: Product packaging improper or incomplete seal of the pouch surrounding the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2020· Smith & Nephew, Inc.

Recalled Item: TWINFIX ULTRA PLLA/HA 6.5 W/3 UB- Absorbable Suture anchor Product Recalled...

The Issue: Product packaging improper or incomplete seal of the pouch surrounding the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2020· Smith & Nephew, Inc.

Recalled Item: OSTEORAPTOR 2.3 W/ 1 UB COBRAID BLACK-Absorbable Suture anchor Product...

The Issue: Product packaging improper or incomplete seal of the pouch surrounding the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2020· Smith & Nephew, Inc.

Recalled Item: OSTEORAPTOR 2.9 W 1UB II BLUE--Absorbable Suture anchor Product Number:...

The Issue: Product packaging improper or incomplete seal of the pouch surrounding the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2020· Smith & Nephew, Inc.

Recalled Item: OSTEORAPTOR 2.9 W. 2 UB WHITE / BLACK -Absorbable Suture Recalled by Smith &...

The Issue: Product packaging improper or incomplete seal of the pouch surrounding the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2020· W L Gore & Associates, Inc.

Recalled Item: GORE TAG CONFORMABLE Thoracic Stent Graft with ACTIVE CONTROL System...

The Issue: Due to secondary deployment fiber being attached to secondary deployment...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2020· Smith & Nephew, Inc.

Recalled Item: OSTEORAPTOR CRVD 2.3 SA UB COBRD BLUE- Absorbable Suture anchor Recalled by...

The Issue: Product packaging improper or incomplete seal of the pouch surrounding the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2020· Smith & Nephew, Inc.

Recalled Item: OSTEORAPTOR CRVD 2.3 SA UB COBRD BLACK- Absorbable Suture anchor Recalled by...

The Issue: Product packaging improper or incomplete seal of the pouch surrounding the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2020· Smith & Nephew, Inc.

Recalled Item: ULTRA FAST-FIX AB ASSEMBLY - CURVED-Absorbable Suture anchors Product...

The Issue: Product packaging improper or incomplete seal of the pouch surrounding the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2020· Smith & Nephew, Inc.

Recalled Item: TWINFIX ULTRA 6.5MM PLLA/HA 2 UBWHT/BL-Absorbable Suture anchor Product...

The Issue: Product packaging improper or incomplete seal of the pouch surrounding the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2020· Smith & Nephew, Inc.

Recalled Item: TWINFIX ULTRA HA 4.5 W/2 UB BLUE & BLK- Absorbable Recalled by Smith &...

The Issue: Product packaging improper or incomplete seal of the pouch surrounding the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2020· GE Healthcare, LLC

Recalled Item: Tomographic Imager Combining Emission Computed Tomography With Nuclear...

The Issue: Potential electrical arc flash within the Power Gradient & RF (PGR) Cabinet.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2020· GE Healthcare, LLC

Recalled Item: System Recalled by GE Healthcare, LLC Due to Potential electrical arc flash...

The Issue: Potential electrical arc flash within the Power Gradient & RF (PGR) Cabinet.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2020· ESAOTE S.P.A

Recalled Item: AC/DC POWER SUPPLY for 7400 Recalled by ESAOTE S.P.A Due to The AC/DC...

The Issue: The AC/DC adapter (power supply) of the portable ultrasound systems listed...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2020· GE Healthcare, LLC

Recalled Item: System Recalled by GE Healthcare, LLC Due to Potential electrical arc flash...

The Issue: Potential electrical arc flash within the Power Gradient & RF (PGR) Cabinet.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2020· ESAOTE S.P.A

Recalled Item: AC/DC POWER SUPPLY for 7400 Recalled by ESAOTE S.P.A Due to The AC/DC...

The Issue: The AC/DC adapter (power supply) of the portable ultrasound systems listed...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2020· GE Healthcare, LLC

Recalled Item: System Recalled by GE Healthcare, LLC Due to Potential electrical arc flash...

The Issue: Potential electrical arc flash within the Power Gradient & RF (PGR) Cabinet.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2020· GE Healthcare, LLC

Recalled Item: System Recalled by GE Healthcare, LLC Due to Potential electrical arc flash...

The Issue: Potential electrical arc flash within the Power Gradient & RF (PGR) Cabinet.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2020· Aesculap Implant Systems LLC

Recalled Item: AESCULAP S4 Cervical Cross Connector L 28-33mm Recalled by Aesculap Implant...

The Issue: Insufficient clamping force of the cross connectors in the spinal surgical...

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

Class II — Potential Health HazardOngoing