Product Recalls in Wyoming

Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,529 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,529 in last 12 months

Showing 1094110960 of 27,462 recalls

Medical DeviceAugust 25, 2020· Genicon, Inc.

Recalled Item: Aquas PowerFlow Tube Set - Product Usage: The device delivers Recalled by...

The Issue: The product design incorporating a motor driven impeller pump powered by one...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2020· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Advanced Perfusion System 1 Ultrasonic Air Sensor 1/4x1/16 UAS BLK...

The Issue: Internal testing at the supplier, revealed that a crimped wire was placed...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2020· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Advanced Perfusion System 1 Ultrasonic Air Sensor 1/4x3/32 Recalled...

The Issue: Internal testing at the supplier, revealed that a crimped wire was placed...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2020· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Advanced Perfusion System 1 Ultrasonic Air Sensor 3/8x3/32 Recalled...

The Issue: Internal testing at the supplier, revealed that a crimped wire was placed...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2020· Boston Scientific Corporation

Recalled Item: Opticross 35 15 MHz Peripheral Imaging Catheter 8F (2.74 mm) Recalled by...

The Issue: Opticross 35 Peripheral Imaging Catheter is being recalled because the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2020· Alcon Research, LLC

Recalled Item: Alcon Custom-Pak Surgical Procedure Packs containing Cardinal Health"...

The Issue: The third-party brand latex micro surgical gloves packaged within specific...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2020· Irvine Biomedical Inc, a St. Jude Medical Co.

Recalled Item: Inquiry Steerable Diagnostic Catheter Recalled by Irvine Biomedical Inc, a...

The Issue: Steerable diagnostic catheter packages labeled Model IBI-81104, batch...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2020· Irvine Biomedical Inc, a St. Jude Medical Co.

Recalled Item: Inquiry Steerable Diagnostic Catheter Recalled by Irvine Biomedical Inc, a...

The Issue: Steerable diagnostic catheter packages labeled Model IBI-81104, batch...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2020· Imactis

Recalled Item: Imactis Patient Fiducial (Patient ) Recalled by Imactis Due to The firm has...

The Issue: The firm has received reports concerning the patient fiducial disk...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2020· Handicare AB

Recalled Item: SwiftHook sold as the following: a. Individually as SwiftHook b. Recalled by...

The Issue: Carry bar may detach during use of mobile lifts and ceiling lifts equipped...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2020· North American Rescue LLC.

Recalled Item: 4 In. Flat Responder Emergency Trauma Dressing part number 30-0171 Recalled...

The Issue: Lack of sterility assurance of the 30-0171

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 20, 2020· Roche Diagnostics Operations, Inc.

Recalled Item: Elecsys Anti-TPO Assay on cobas e analyzers 411 Recalled by Roche...

The Issue: Recent internal verification studies found the current RF interference claim...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2020· Ansell Healthcare Products LLC

Recalled Item: MICROFLEX Diamond Grip Examination Gloves Recalled by Ansell Healthcare...

The Issue: Examination gloves were shipped inadvertently, without to verify barrier...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension LOCI High Sensitivity Troponin I (TNIH) Flex reagent...

The Issue: Positive bias across the Analytical Measurement Range of the TNIH assay...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Software: Syngo.via RT Image Suite software version VA30_SP02 with license...

The Issue: Calibration offset between the central CT image plane and the external RT...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2020· Ameditech Inc

Recalled Item: Consult Diagnostics Drugs Abuse Test Cup (AMT Item Number/ AMT Recalled by...

The Issue: Various immunoassay enzymes failed product performance, thereby the products...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2020· Beckman Coulter Inc.

Recalled Item: UIBC Recalled by Beckman Coulter Inc. Due to The manufacturer has identified...

The Issue: The manufacturer has identified that the use of Unsaturated Iron Binding...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2020· Ameditech Inc

Recalled Item: ToxCup Drug Screen Cup (AMT Item Number/ AMT Description): HT29A/"ToxCup¿...

The Issue: Various immunoassay enzymes failed product performance, thereby the products...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2020· Ameditech Inc

Recalled Item: First Check 7 Panel Drug Cup: (AMP/COC/MDMA/MET/OPI/PCP/THC) Recalled by...

The Issue: Various immunoassay enzymes failed product performance, thereby the products...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2020· Ameditech Inc

Recalled Item: Noble 1 Step+ Cup (AMT Item Number/ AMT Description): NBCA-13A-B Recalled by...

The Issue: Various immunoassay enzymes failed product performance, thereby the products...

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

Class II — Potential Health HazardOngoing