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. 1,173 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
1,173 in last 12 months

Showing 6481–6500 of 30,921 recalls

Medical DeviceMay 19, 2023· Olympus Corporation of the Americas

Recalled Item: UroPass Ureteral Access Sheaths Recalled by Olympus Corporation of the...

The Issue: Dilator tips may break in the package and in patients during surgical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2023· Qiagen GmbH

Recalled Item: QIAstat-Dx Respiratory SARS-CoV-2 Panel (V1 and V2 Recalled by Qiagen GmbH...

The Issue: Identified a decreased performance reliability rate, Run abortions could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2023· Qiagen GmbH

Recalled Item: QIAstat-Dx Respiratory SARS-CoV-2 Panel -US IVD qualitative test intended...

The Issue: Identified a decreased performance reliability rate, Run abortions could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2023· Baxter Healthcare Corporation

Recalled Item: Voalte Patient Safety Recalled by Baxter Healthcare Corporation Due to...

The Issue: Baxter identified a potential risk where the "safety" monitoring and "bed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2023· Baxter Healthcare Corporation

Recalled Item: NaviCare Patient Safety V3.9.200 to 3.9.600 Recalled by Baxter Healthcare...

The Issue: Baxter identified a potential risk where the "safety" monitoring and "bed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2023· Philips North America Llc

Recalled Item: DigitalDiagnost C90 Recalled by Philips North America Llc Due to There is a...

The Issue: There is a software login in issue that may prevent the user from logging in.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Probe Cover Kits containing sterile Ultrasound Gel Recalled by...

The Issue: Probe covers for use during diagnostic ultrasound procedures may have an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Probe Cover Kits containing sterile Ultrasound Gel Recalled by...

The Issue: Probe covers for use during diagnostic ultrasound procedures may have an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Probe Cover Kits containing sterile Ultrasound Gel Recalled by...

The Issue: Probe covers for use during diagnostic ultrasound procedures may have an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Probe Cover Kits containing sterile Ultrasound Gel Recalled by...

The Issue: Probe covers for use during diagnostic ultrasound procedures may have an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Probe Cover Kits containing sterile Ultrasound Gel Recalled by...

The Issue: Probe covers for use during diagnostic ultrasound procedures may have an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Probe Cover Kits containing sterile Ultrasound Gel Recalled by...

The Issue: Probe covers for use during diagnostic ultrasound procedures may have an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Probe Cover Kits containing sterile Ultrasound Gel Recalled by...

The Issue: Probe covers for use during diagnostic ultrasound procedures may have an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Probe Cover Kits containing sterile Ultrasound Gel Recalled by...

The Issue: Probe covers for use during diagnostic ultrasound procedures may have an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· Maquet Medical Systems USA

Recalled Item: QUADROX-i Small Adult Recalled by Maquet Medical Systems USA Due to Product...

The Issue: Product packaging may exhibit small pinholes which may not be visible to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· Maquet Medical Systems USA

Recalled Item: QUADROX-iR Recalled by Maquet Medical Systems USA Due to 1. An accessory may...

The Issue: 1. An accessory may be improperly placed during packaging, causing creases...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· Maquet Medical Systems USA

Recalled Item: QUADROX-i Adult Recalled by Maquet Medical Systems USA Due to 1. An...

The Issue: 1. An accessory may be improperly placed during packaging, causing creases...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· Maquet Medical Systems USA

Recalled Item: QUADROX-i Pediatric Recalled by Maquet Medical Systems USA Due to Product...

The Issue: Product packaging may exhibit small pinholes which may not be visible to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Probe Cover Kits containing sterile Ultrasound Gel Recalled by...

The Issue: Probe covers for use during diagnostic ultrasound procedures may have an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· Aesculap Implant Systems LLC

Recalled Item: Aesculap Surgical Needle Recalled by Aesculap Implant Systems LLC Due to...

The Issue: Incorrect product code marked on the product, etched with product code...

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

Class II — Potential Health HazardOngoing