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 1106111080 of 27,462 recalls

Medical DeviceJuly 31, 2020· Klarity Medical Products LLC

Recalled Item: Klarity Vacuum Bags Recalled by Klarity Medical Products LLC Due to Vacuum...

The Issue: Vacuum bags potentially may not hold their vacuum adequately for needed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2020· Thera Test Laboratories, Inc.

Recalled Item: EL-Anti-SARS-CoV-2 IgM Kit Recalled by Thera Test Laboratories, Inc. Due to...

The Issue: Device did not meet the updated EUA packet requirements for positive percent...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2020· CME America, LLC

Recalled Item: CME America T-Syringe Pump - T34 - Product Usage: infusion Recalled by CME...

The Issue: Multiple reasons: 1) Due to wear and tear of pump motor block mechanism -...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2020· CME America, LLC

Recalled Item: CME America T-Syringe Pump - T34L PCA - Product Usage: Recalled by CME...

The Issue: Multiple reasons: 1) Due to wear and tear of pump motor block mechanism -...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2020· CME America, LLC

Recalled Item: CME America T-Syringe Pump - Neofeed - Product Usage: infusion Recalled by...

The Issue: Multiple reasons: 1) Due to wear and tear of pump motor block mechanism -...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2020· CME America, LLC

Recalled Item: CME America T-Syringe Pump - Ameritus 1st Enteral Pump - Recalled by CME...

The Issue: Multiple reasons: 1) Due to wear and tear of pump motor block mechanism -...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2020· CME America, LLC

Recalled Item: CME America T-Syringe Pump - NeoThrive - Product Usage: infusion Recalled by...

The Issue: Multiple reasons: 1) Due to wear and tear of pump motor block mechanism -...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2020· CME America, LLC

Recalled Item: CME America T-Syringe Pump -T34L - Product Usage: infusion of Recalled by...

The Issue: Multiple reasons: 1) Due to wear and tear of pump motor block mechanism -...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2020· Cardinal Health 200, LLC

Recalled Item: KIT Recalled by Cardinal Health 200, LLC Due to Only providing one nasal...

The Issue: Only providing one nasal swab in our pre-operative kit instead of the 4...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2020· Sorin Group Italia S.r.l.

Recalled Item: Perceval Single Use Accessory Kit Recalled by Sorin Group Italia S.r.l. Due...

The Issue: LivaNova received complaints indicating the impossibility to collapse...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2020· Sorin Group Italia S.r.l.

Recalled Item: Perceval Single Use Accessory Kit Recalled by Sorin Group Italia S.r.l. Due...

The Issue: LivaNova received complaints indicating the impossibility to collapse...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2020· Sorin Group Italia S.r.l.

Recalled Item: Perceval Dual Collapser Recalled by Sorin Group Italia S.r.l. Due to...

The Issue: LivaNova received complaints indicating the impossibility to collapse...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2020· Sorin Group Italia S.r.l.

Recalled Item: Perceval Single Use Accessory Kit Recalled by Sorin Group Italia S.r.l. Due...

The Issue: LivaNova received complaints indicating the impossibility to collapse...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2020· Sorin Group Italia S.r.l.

Recalled Item: Perceval Single Use Accessory Kit Recalled by Sorin Group Italia S.r.l. Due...

The Issue: LivaNova received complaints indicating the impossibility to collapse...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2020· Cardinal Health 200, LLC

Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 6.0 - Product Usage: Recalled by...

The Issue: A degradation defect was found that could lead to holes and donning tears at...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2020· Cardinal Health 200, LLC

Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 8.5 - Product Usage: Recalled by...

The Issue: A degradation defect was found that could lead to holes and donning tears at...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2020· Cardinal Health 200, LLC

Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 7.5 - Product Usage: Recalled by...

The Issue: A degradation defect was found that could lead to holes and donning tears at...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2020· Cardinal Health 200, LLC

Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 5.5 - Product Usage: Recalled by...

The Issue: A degradation defect was found that could lead to holes and donning tears at...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2020· Cardinal Health 200, LLC

Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 8.0 - Product Usage: Recalled by...

The Issue: A degradation defect was found that could lead to holes and donning tears at...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2020· Cardinal Health 200, LLC

Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 9.0 - Product Usage: Recalled by...

The Issue: A degradation defect was found that could lead to holes and donning tears at...

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

Class II — Potential Health HazardOngoing