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. 2,535 recalls have been distributed to Wyoming in the last 12 months.
Showing 9061–9080 of 27,462 recalls
Recalled Item: Catalog A303318A Recalled by C.R. Bard Inc Due to There is potential for...
The Issue: There is potential for packaging defects that may impact the sterile barrier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMSORB PLUS PREFILLED G-CAN 1.0L Recalled by Armstrong Medical Services...
The Issue: Some devices may be associated with high and unexpected resistance to gas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalog A300318A Recalled by C.R. Bard Inc Due to There is potential for...
The Issue: There is potential for packaging defects that may impact the sterile barrier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalog A303316A Recalled by C.R. Bard Inc Due to There is potential for...
The Issue: There is potential for packaging defects that may impact the sterile barrier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalog A943216 Recalled by C.R. Bard Inc Due to There is potential for...
The Issue: There is potential for packaging defects that may impact the sterile barrier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalog A800361 Recalled by C.R. Bard Inc Due to There is potential for...
The Issue: There is potential for packaging defects that may impact the sterile barrier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalog A800365 Recalled by C.R. Bard Inc Due to There is potential for...
The Issue: There is potential for packaging defects that may impact the sterile barrier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: General Manual surgical instrument Recalled by M.D.L. S.r.l. Due to...
The Issue: Sterility assurance may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalog A300314A Recalled by C.R. Bard Inc Due to There is potential for...
The Issue: There is potential for packaging defects that may impact the sterile barrier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalog A902916 Recalled by C.R. Bard Inc Due to There is potential for...
The Issue: There is potential for packaging defects that may impact the sterile barrier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aspirated Cyto-Histological Biopsy needle Recalled by M.D.L. S.r.l. Due to...
The Issue: Sterility assurance may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 0.9% Sodium Chloride Flush Syringe Recalled by Cardinal Health Due...
The Issue: Potential for the plunger to draw back after the air has been expelled and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vysis CLL FISH Probe Kit with the following components: Vysis Recalled by...
The Issue: Potential for Vysis CLL FISH Probe Kits not detecting 13q deletions in known...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas SARS-CoV-2 & Influenza A/B Test for use on the cobas Liat System...
The Issue: Customers have reported an increased number of false positive SARS-CoV-2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 0.9% Sodium Chloride Flush Syringe Recalled by Cardinal Health Due...
The Issue: Potential for the plunger to draw back after the air has been expelled and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 0.9% Sodium Chloride Flush Syringe Recalled by Cardinal Health Due...
The Issue: Potential for the plunger to draw back after the air has been expelled and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultrasound Gel labeled under the following brand names: MediChoice...
The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verigene EP Amplification Reagent Kit Test Recalled by Luminex Corporation...
The Issue: There is potential for false positive results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arc Endocuff Vision as follows: ARV110 ENDOCUFF-V M BLUE PK8 Recalled by...
The Issue: Packaging seal defect may allow a breach of the package sterile barrier and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AquaBplus Water Purification System Recalled by Fresenius Medical Care...
The Issue: AquaBplus HF module on the AquaBplus 2000 osmosis system, an error in the US...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.