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. 1,077 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
1,077 in last 12 months

Showing 2461–2480 of 27,462 recalls

Medical DeviceNovember 25, 2024· Olympus Corporation of the Americas

Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...

The Issue: The probe tips of the hand instruments are being damaged or breaking...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2024· Olympus Corporation of the Americas

Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...

The Issue: The probe tips of the hand instruments are being damaged or breaking...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2024· Olympus Corporation of the Americas

Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...

The Issue: The probe tips of the hand instruments are being damaged or breaking...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2024· Olympus Corporation of the Americas

Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...

The Issue: The probe tips of the hand instruments are being damaged or breaking...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2024· Angiodynamics, Inc.

Recalled Item: AURYON LASER SYSTEM 100-120 VAC. Model Number: EXM001. Product Number:...

The Issue: Potential for procedural delays or interruptions during use of the Auryon...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2024· Olympus Corporation of the Americas

Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...

The Issue: The probe tips of the hand instruments are being damaged or breaking...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2024· Olympus Corporation of the Americas

Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...

The Issue: The probe tips of the hand instruments are being damaged or breaking...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2024· Olympus Corporation of the Americas

Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...

The Issue: The probe tips of the hand instruments are being damaged or breaking...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2024· Olympus Corporation of the Americas

Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...

The Issue: The probe tips of the hand instruments are being damaged or breaking...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2024· Olympus Corporation of the Americas

Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...

The Issue: The probe tips of the hand instruments are being damaged or breaking...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 24, 2024· Adept Medical Ltd

Recalled Item: Otological Ventilation Tube - T-Tube 12mm - Double - Silicone Recalled by...

The Issue: Lack of 510(k) clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 24, 2024· Adept Medical Ltd

Recalled Item: Otological Ventilation Tube - T-Tube 9mm - Silicone Recalled by Adept...

The Issue: Lack of 510(k) clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 24, 2024· Adept Medical Ltd

Recalled Item: Otological Ventilation Tube - T-Tube 6mm - Double - Silicone Recalled by...

The Issue: Lack of 510(k) clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 24, 2024· Adept Medical Ltd

Recalled Item: Otological Ventilation Tube - Donaldson - Blue Silicone Recalled by Adept...

The Issue: Lack of 510(k) clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 24, 2024· Adept Medical Ltd

Recalled Item: Otological Ventilation Tube - T-Tube 9mm - Double - Silicone Recalled by...

The Issue: Lack of 510(k) clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 24, 2024· Adept Medical Ltd

Recalled Item: Otological Ventilation Tube - T-Tube 12mm - Silicone Recalled by Adept...

The Issue: Lack of 510(k) clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 24, 2024· Adept Medical Ltd

Recalled Item: Otological Ventilation Tube - T-Tube 6mm - Silicone Recalled by Adept...

The Issue: Lack of 510(k) clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 24, 2024· Adept Medical Ltd

Recalled Item: Otological Ventilation Tube - Donaldson - Double - Blue Silicone Recalled by...

The Issue: Lack of 510(k) clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2024· 3M Company - Health Care Business

Recalled Item: Clarity Precision Grip Attachments Recalled by 3M Company - Health Care...

The Issue: Attachments may not mate with the tooth as intended in the digital treatment...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: epoc NXS Host Recalled by Siemens Healthcare Diagnostics, Inc. Due to...

The Issue: Siemens Healthcare Diagnostics is recalling their epoc Blood Analysis System...

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

Class II — Potential Health HazardOngoing