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. 2,486 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,486 in last 12 months

Showing 1614116160 of 27,462 recalls

Medical DeviceJanuary 23, 2018· 3M Company - Health Care Business

Recalled Item: 3M Bair Hugger(M) Normothermia System Recalled by 3M Company - Health Care...

The Issue: Adesign change to 3M(TM) Bair Hugger(TM) Full Access Underbody Warming...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 23, 2018· Biomerieux Inc

Recalled Item: bioM¿rieux VITEK 2 NH ID Test Kit Product Usage: Is Recalled by Biomerieux...

The Issue: Missing desiccant.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 22, 2018· Valeris Medical, LLC

Recalled Item: Apollo XT Suture Anchor Recalled by Valeris Medical, LLC Due to The label on...

The Issue: The label on Apollo XT 5.5mm Suture Anchor (part # XTS-5515; lots 2358,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2018· SIE AG, Surgical Instrument Engineering

Recalled Item: The FEMTO LDV(TM)Z8 Femtosecond Surgical Laser The FEMTO LDV(TM)Z8...

The Issue: This Correction is being initiated based on a customer complaint received on...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2018· Beckman Coulter Inc.

Recalled Item: AutoMate 2550 "High Speed" Catalog Number ODL25255 Recalled by Beckman...

The Issue: A misaligned pipette tip sensor poses the remote risk of cross-contamination...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2018· Olympus Corporation of the Americas

Recalled Item: Uretero-reno videoscope URF-V2 Uretero-reno videoscope URF-V2R Recalled by...

The Issue: Potential breakage of the endoscope s insertion tube bending section during...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2018· Olympus Corporation of the Americas

Recalled Item: Uretero-reno fiberscope URF-P6 Recalled by Olympus Corporation of the...

The Issue: Breakage of the endoscope's insertion tube bending section during surgical...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2018· Olympus Corporation of the Americas

Recalled Item: Uretero-reno fiberscope URF-P6RP6 Recalled by Olympus Corporation of the...

The Issue: Breakage of the endoscope's insertion tube bending section during surgical...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 12, 2018· Beckman Coulter Inc.

Recalled Item: COULTER EPICS XL Flow Cytometer COULTER EPICS XL-MCL Flow Cytometer Recalled...

The Issue: A manufacturing defect on the amplifier board of the Flow Cytometers my...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 12, 2018· Beckman Coulter Inc.

Recalled Item: 1) Cytomics FC 500 With CXP Software BECKMAN COULTER 2) Recalled by Beckman...

The Issue: A manufacturing defect on the amplifier board of the Flow Cytometers my...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 12, 2018· Hill-Rom, Inc.

Recalled Item: Progressa Bed - AC-powered adjustable hospital bed Recalled by Hill-Rom,...

The Issue: A component used within the braking system may break resulting in one or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 12, 2018· Shimadzu Medical Systems

Recalled Item: Sonialvision Safire II Recalled by Shimadzu Medical Systems Due to When...

The Issue: When selecting serial radiography with a pulse rate of 7.5fps (including...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 12, 2018· Cook Inc.

Recalled Item: MINC Benchtop Incubator (Mini Incubator) catalog (K-MINC-1000 US) G46022 is...

The Issue: The temperature of the incubation lids of the MINC Bench top Incubators may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 12, 2018· Cook Inc.

Recalled Item: MINC Benchtop Incubator (Mini Incubator) catalog (K-MINC-1000) G20079 is a...

The Issue: The temperature of the incubation lids of the MINC Bench top Incubators may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2018· GE Medical Systems Information Technologies, Inc.

Recalled Item: GE HEALTHCARE CARESCAPE Central Station (CSCS) software version 2.0.2 The...

The Issue: CARESCAPE Central Station (CSCS) software version 2.0.2 units may experience...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2018· Ellex iScience, Inc.

Recalled Item: ellex I.Science iTRACK 250A Recalled by Ellex iScience, Inc. Due to...

The Issue: Sterility failure found in one of the units in the lot.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2018· Ethicon, Inc.

Recalled Item: PDS Plus Antibacterial (Polydioxanone) Suture Size 0 PDS Plus Violet...

The Issue: Three (3) lots were distributed with the incorrect expiry date on the label....

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2018· Ethicon, Inc.

Recalled Item: PDS Plus Antibacterial (Polydioxanone) Suture Size 1 PDS PLUS Violet...

The Issue: Three (3) lots were distributed with the incorrect expiry date on the label....

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2018· Ethicon, Inc.

Recalled Item: PDS Plus Antibacterial (Polydioxanone) Suture Size 0 PDS Plus Violet...

The Issue: Three (3) lots were distributed with the incorrect expiry date on the label....

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2018· Riverpoint Medical, LLC

Recalled Item: RP RIVERPOINT MEDICAL 18G Brachy Grid B&K(TM) style Recalled by Riverpoint...

The Issue: Product is labeled with "CE", but is not yet approved in the European Union.

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

Class III — Low RiskOngoing