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. 2,540 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,540 in last 12 months

Showing 64416460 of 27,462 recalls

Medical DeviceApril 25, 2023· BioFire Diagnostics, LLC

Recalled Item: FILMARRAY Gastrointestinal (GI) Panel (Part No.: RFIT-ASY-0104 &...

The Issue: The firm has identified an increased risk of obtaining false positive...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2023· Philips North America

Recalled Item: Incisive CT-Computed Tomography X-Ray System Model: 728143 Recalled by...

The Issue: Metal mounting box on the rotating scanner on rotor (heat exchanger box)...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2023· Linkbio Corp.

Recalled Item: LINK SymphoKnee System L-Shaped Femoral Augment Recalled by Linkbio Corp....

The Issue: Contains the incorrect implant in the packaging. The packaging incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2023· Philips North America

Recalled Item: Incisive CT Power (China)-Computed Tomography X-Ray System Model: 728148...

The Issue: Metal mounting box on the rotating scanner on rotor (heat exchanger box)...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2023· Philips North America

Recalled Item: Incisive CT Plus-Computed Tomography X-Ray System Model: 728149 Recalled by...

The Issue: Metal mounting box on the rotating scanner on rotor (heat exchanger box)...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2023· Davol, Inc.

Recalled Item: Ventralight ST w Echo PS 4.5" Circle A low profile Recalled by Davol, Inc....

The Issue: Balloon may not inflate as intended. If the balloon does not inflate during...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2023· Davol, Inc.

Recalled Item: Ventralight ST w EchoPS 4"x6" Ellipse- A low profile Recalled by Davol, Inc....

The Issue: Balloon may not inflate as intended. If the balloon does not inflate during...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2023· Davol, Inc.

Recalled Item: Ventralight ST 4" x 6" Ellipse with Echo PS Catalog Number: 5955460 Recalled...

The Issue: Balloon may not inflate as intended. If the balloon does not inflate during...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2023· LumiraDx

Recalled Item: SteriPack Sterile Polyester Spun Swabs (25 units/Pack)- Intended for sample...

The Issue: Fails Post-Sterilization Sterile Swabs Cantilever (Bend) Testing and may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2023· Avanos Medical, Inc.

Recalled Item: AVNS ambIT System - PIB/PCA W 5in Cath Recalled by Avanos Medical, Inc. Due...

The Issue: Some of the ambIT kits were potentially distributed without an air in-line...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2023· Cepheid

Recalled Item: Xpert Xpress Strep A Recalled by Cepheid Due to pipettes packaged in Strep A...

The Issue: pipettes packaged in Strep A test may fail to dispense an adequate sample...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2023· Cepheid

Recalled Item: Xpert Xpress Strep A Recalled by Cepheid Due to pipettes packaged in Strep A...

The Issue: pipettes packaged in Strep A test may fail to dispense an adequate sample...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2023· Avanos Medical, Inc.

Recalled Item: ambIT Cassette Filter Male Luer Recalled by Avanos Medical, Inc. Due to Some...

The Issue: Some of the ambIT kits were potentially distributed without an air in-line...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2023· Avanos Medical, Inc.

Recalled Item: SMMT ambIT Kit Basic Filter Luer Cass Recalled by Avanos Medical, Inc. Due...

The Issue: Some of the ambIT kits were potentially distributed without an air in-line...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2023· Abbott Ireland Limited

Recalled Item: Alinity i Anti-TPO Reagent Kit Recalled by Abbott Ireland Limited Due to Due...

The Issue: Due to a manufacturing fill volume error, Alinity i Anti-TPO Reagent...

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

Class III — Low RiskOngoing
Medical DeviceApril 24, 2023· Avanos Medical, Inc.

Recalled Item: AVNS ambIT System - PIB/PCA W 2.5in Cath Recalled by Avanos Medical, Inc....

The Issue: Some of the ambIT kits were potentially distributed without an air in-line...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2023· Avanos Medical, Inc.

Recalled Item: SMMT ambIT Reusable Program - Luer Cass Recalled by Avanos Medical, Inc. Due...

The Issue: Some of the ambIT kits were potentially distributed without an air in-line...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2023· Merit Medical Systems, Inc.

Recalled Item: Aspira Drainage Catheter Insertion Tray 15.5F Recalled by Merit Medical...

The Issue: There is a potential that valve assemblies will not open. preventing fluid...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2023· Merit Medical Systems, Inc.

Recalled Item: Aspira Drainage Catheter Insertion Tray 15.5F Recalled by Merit Medical...

The Issue: There is a potential that valve assemblies will not open. preventing fluid...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2023· Merit Medical Systems, Inc.

Recalled Item: Aspira Pleural Drainage Catheter Insertion Tray 15.5F Recalled by Merit...

The Issue: There is a potential that valve assemblies will not open. preventing fluid...

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

Class II — Potential Health HazardOngoing