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. 1,053 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
1,053 in last 12 months

Showing 10921–10940 of 27,462 recalls

Medical DeviceAugust 31, 2020· ICU Medical, Inc.

Recalled Item: 30" (76 cm) Appx 5.5 mL 20 Drop Admin Set w/Integrated Clave Drip Chamber...

The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2020· Ultradent Products, Inc.

Recalled Item: PermaFlo Flowable Composite 948 Shade: A2 - Product Usage: Recalled by...

The Issue: Due to a potential manufacturing issue (cross contamination), composite is...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2020· ICU Medical, Inc.

Recalled Item: 3mL Syringe w/Spinning Spiros Recalled by ICU Medical, Inc. Due to Potential...

The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2020· Cook Inc.

Recalled Item: Percutaneous Neonatal Pigtail Nephrostomy Set Recalled by Cook Inc. Due to...

The Issue: The indwell time for the Percutaneous Neonatal Pigtail Nephrostomy Set and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2020· Vascular Solutions, Inc.

Recalled Item: Langston Dual Lumen Catheter. Recalled by Vascular Solutions, Inc. Due to...

The Issue: The inner lumen of the Langston catheter may separate from the hub during...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 31, 2020· ICU Medical, Inc.

Recalled Item: Spinning Spiros Recalled by ICU Medical, Inc. Due to Potential for spinning...

The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2020· Vascular Solutions, Inc.

Recalled Item: Langston Dual Lumen Catheter. Recalled by Vascular Solutions, Inc. Due to...

The Issue: The inner lumen of the Langston catheter may separate from the hub during...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 31, 2020· ICU Medical, Inc.

Recalled Item: 76 cm (30") Appx 3.3 ml Recalled by ICU Medical, Inc. Due to Potential for...

The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2020· Vascular Solutions, Inc.

Recalled Item: Langston Dual Lumen Catheter Recalled by Vascular Solutions, Inc. Due to The...

The Issue: The inner lumen of the Langston catheter may separate from the hub during...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 31, 2020· ICU Medical, Inc.

Recalled Item: Spiros CLOSED MALE LUER w/RED CAP Recalled by ICU Medical, Inc. Due to...

The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2020· Greiner Bio-One North America, Inc.

Recalled Item: VACUETTE TUBE 5 mL CAT Serum Separator Clot Activator Recalled by Greiner...

The Issue: Blood collection tubes experienced an issue with separation and clotting

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2020· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens epoc BGEM Test Card-In vitro diagnostic device for the Recalled by...

The Issue: Sporadically inconsistent discrepant (low bias) glucose results on card lot...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 27, 2020· Roche Diagnostics Operations, Inc.

Recalled Item: Tina-quant Complement C4 ver.2 Recalled by Roche Diagnostics Operations,...

The Issue: Roche has confirmed customer complaints of low quality (QC) recovery and...

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

Class III — Low RiskOngoing
Medical DeviceAugust 27, 2020· Roche Diagnostics Operations, Inc.

Recalled Item: Albumin Gen.2 Recalled by Roche Diagnostics Operations, Inc. Due to Roche...

The Issue: Roche has confirmed customer complaints of low quality (QC) recovery and...

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

Class III — Low RiskOngoing
Medical DeviceAugust 26, 2020· Beckman Coulter Inc.

Recalled Item: BECKMAN COULTER ACCESS Immunoassay Systems - Access Unconjugated Estriol...

The Issue: Due to alkaline phosphatase (ALP) associated interference causing falsely...

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 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 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· 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· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Dimension Vista Akaline Phosphatase (ALPI) Flex reagent cartridge -...

The Issue: Low outlier resultsgenerated with Alkaline Phosphatase (ALPI) Flex reagent...

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

Class II — Potential Health HazardOngoing