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 61016120 of 30,921 recalls

Medical DeviceJuly 10, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica¿ CH HDL Cholesterol- In vitro diagnostic use in the Recalled by...

The Issue: Potential for reagent carryover on the Atellica CH 930 resulting in a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Total Bilirubin_2 -In vitro diagnostic use in the Recalled by...

The Issue: Potential for reagent carryover on the Atellica CH 930 resulting in a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2023· Stryker Corporation

Recalled Item: SurgiCount+ Software Application-indicated as an adjunctive technology for...

The Issue: Potential for current software to miscount when scanning in multiple...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH LDL Cholesterol- In vitro diagnostic use in the Recalled by...

The Issue: Potential for reagent carryover on the Atellica CH 930 resulting in a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2023· Karl Storz Endoscopy

Recalled Item: Five S 5 3x65 Recalled by Karl Storz Endoscopy Due to Flexible intubation...

The Issue: Flexible intubation endoscopes sterility assurance can not be confirmed.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2023· Alphatec Spine, Inc.

Recalled Item: LIF AMP Recalled by Alphatec Spine, Inc. Due to Awl instrument adjustable...

The Issue: Awl instrument adjustable drill button assembly assembled in the incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2023· Aquila Corporation

Recalled Item: APK2 Pressure-Sensing Wheelchair Cushions Recalled by Aquila Corporation Due...

The Issue: Defective battery pack in wheelchair cushions can overheat resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2023· Aquila Corporation

Recalled Item: SofTech Pressure-Sensing Wheelchair Cushions Recalled by Aquila Corporation...

The Issue: Defective battery pack in wheelchair cushions can overheat resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2023· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...

The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2023· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...

The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2023· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...

The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Total Hip Kit Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to The...

The Issue: The prep solution included in the Total Hip Kit expires prior to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2023· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...

The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2023· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...

The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2023· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...

The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2023· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...

The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2023· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...

The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2023· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...

The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2023· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...

The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2023· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...

The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...

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

Class II — Potential Health HazardOngoing