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. 2,404 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,404 in last 12 months

Showing 2108121100 of 48,219 recalls

Medical DeviceJune 12, 2019· Becton Dickinson & Company

Recalled Item: BD Vacutainer Lithium HeparinN (LH) 95 USP Units Blood Collection Tubes...

The Issue: False elevation of carboxyhemoglobin (COHb) results have been reported when...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2019· Randox Laboratories, Limited

Recalled Item: Human Assayed Multi-Sera Level 2 Recalled by Randox Laboratories, Limited...

The Issue: The RX Series control target and range value for ALT (Tris buffer without...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2019· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView XCT Recalled by Philips Medical Systems (Cleveland) Inc Due to An...

The Issue: An issue with the handcontroller may result in either spontaneous...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2019· Molded Products Inc

Recalled Item: Luer Lock Set - Catalog # MPC-125 Recalled by Molded Products Inc Due to...

The Issue: Mislabeling - Some unit of sale packages (bags of 100 sets of MPC-125) were...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2019· Zimmer Biomet, Inc.

Recalled Item: Comprehensive Reverse Shoulder Instrument Case Outer (Outer Case Vault Only)...

The Issue: Lack of an adequate sterilization validation.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2019· Abbott Gmbh & Co. KG

Recalled Item: Alinity ci -series System Control¿Module Recalled by Abbott Gmbh & Co. KG...

The Issue: Abbott has identified an issue with all on market versions (v2.6.0 and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2019· Olympus Corporation of the Americas

Recalled Item: Olympus WM-NP2 or WM-DP2 Mobile Workstations with Nurse Control Panel Arm...

The Issue: WM-NP/DP2 workstations could become unstable and may fall over if the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2019· Zimmer Biomet, Inc.

Recalled Item: Comprehensive Reverse Shoulder Instrument Case Total (Outer Case Vault Only)...

The Issue: Lack of an adequate sterilization validation.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2019· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView X Recalled by Philips Medical Systems (Cleveland) Inc Due to An...

The Issue: An issue with the handcontroller may result in either spontaneous...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2019· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView SPECT Recalled by Philips Medical Systems (Cleveland) Inc Due to...

The Issue: An issue with the handcontroller may result in either spontaneous...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2019· Burlington Medical, LLC

Recalled Item: Frontal Apron with Quick Drop Velcro Closure (no elastic) Recalled by...

The Issue: The protective material used in the manufacture of the products could...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2019· Burlington Medical, LLC

Recalled Item: Thyroid Collar Recalled by Burlington Medical, LLC Due to The protective...

The Issue: The protective material used in the manufacture of the products could...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2019· Burlington Medical, LLC

Recalled Item: Frontal Apron Velcro Closure Recalled by Burlington Medical, LLC Due to The...

The Issue: The protective material used in the manufacture of the products could...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2019· Burlington Medical, LLC

Recalled Item: Porta Shield Recalled by Burlington Medical, LLC Due to The protective...

The Issue: The protective material used in the manufacture of the products could...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2019· Burlington Medical, LLC

Recalled Item: 2 pc Full Wrap Vest & Kilt Back-Saver Recalled by Burlington Medical, LLC...

The Issue: The protective material used in the manufacture of the products could...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2019· Burlington Medical, LLC

Recalled Item: Vest Recalled by Burlington Medical, LLC Due to The protective material used...

The Issue: The protective material used in the manufacture of the products could...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2019· Burlington Medical, LLC

Recalled Item: Peak Vest Recalled by Burlington Medical, LLC Due to The protective material...

The Issue: The protective material used in the manufacture of the products could...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2019· Burlington Medical, LLC

Recalled Item: Overlap Vest Recalled by Burlington Medical, LLC Due to The protective...

The Issue: The protective material used in the manufacture of the products could...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2019· Burlington Medical, LLC

Recalled Item: Cap Recalled by Burlington Medical, LLC Due to The protective material used...

The Issue: The protective material used in the manufacture of the products could...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2019· Burlington Medical, LLC

Recalled Item: Frontal Stretch Buckle Closure Apron Recalled by Burlington Medical, LLC Due...

The Issue: The protective material used in the manufacture of the products could...

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

Class II — Potential Health HazardOngoing