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. 2,292 recalls have been distributed to Wyoming in the last 12 months.
Showing 42761–42780 of 48,219 recalls
Recalled Item: VITROS CA 125 II Calibrators For use in the calibration Recalled by...
The Issue: Ortho Clinical Diagnostics issued a Product Correction Notification for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Transradial Artery Access products Arrow Transradial Artery Access...
The Issue: There is a risk that the introducer needles packaged within the kits can be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes TomoFix Plates The Synthes J5606-C TomoFix Osteotomy System is...
The Issue: A labeling correction was initiated related to the Surgical Technique Guide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trinica Anterior Lumbar Plate (ALP) system Recalled by Zimmer, Inc. Due to...
The Issue: Zimmer Spine, Inc. is initiating a correction regarding the Trinica ALP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: White grits packaged in a paper bag labeled in part: Smooth & Creamy...
The Issue: Some Aunt Jemima brand Buttermilk Self-Rising Corn Meal Mix, Quick Grits...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: White grits packaged in a paper bag labeled in part: Smooth & Creamy...
The Issue: Aflatoxins. Some Aunt Jemima brand Buttermilk Self-Rising Corn Meal Mix,...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: enGen Track System with enGen Select v5.0 with autoverification enabled...
The Issue: Ortho Clinical Diagnostics issued an Urgent Product Correction Notification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: enGen Track System with enGen Custom v3.2.2 (& below) Product The VITROS 5...
The Issue: Ortho Clinical Diagnostics issued an Urgent Product Correction Notification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Implant Holder for Synfix (TM)-LR the Synthes Implant Holder...
The Issue: Complaints were received which described the SynFix LR implant holder...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Slim Fortune capsules Dietary Supplement. Each bottle contains 30 capsules....
The Issue: Marketed Without an Approved NDA/ANDA; product found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Slim Expert softgel capsules Dietary Supplement. One month supply/ 30...
The Issue: Marketed Without an Approved NDA/ANDA; product found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidiy capsules Dietary Supplement. Each bottle contains 30 capsules....
The Issue: Marketed Without an Approved NDA/ANDA; product found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dexedrine¿ (Dextroamphetamine Sulfate) Spansules¿ Sustained Release Capsules...
The Issue: Failed Dissolution Specifications: Out of Specification (OOS) test results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 1) The HomeChoice automated peritoneal dialysis system. Dataplate located on...
The Issue: In systems with version 10.4 software Initial Drain logic, the device will...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARINAsim MAN-1236 Rev 2 and CARINAiso MAN-1237 Rev 2 laser Recalled by LAP...
The Issue: Potential for patient to be marked incorrectly. Customers currently using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: User Defined Method Flex Assignment/Siemens Dimension Vista 500 or Dimension...
The Issue: When utilizing the Routine Inventory screen to enter a User Defined Method...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C-Plus" 10mm x 12mm Webless implants Pioneer Surgical's C-Plus " Recalled by...
The Issue: As the result of a recent internal review of regulatory documents, we have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multi Parameter Patient Monitor (with Arrhythmia Detection and Alarms)...
The Issue: Mindray has identified an issue with V Series Monitor where the V Dock power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GENESIS(R) II Recalled by Smith & Nephew Inc Due to Swapped product....
The Issue: Swapped product. Non-porous tibial base size 5 L was mis-packaged as size 6...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Resolute Integrity Zotarolimus-eluting Coronary Stent: Stent ID 3.0 mm...
The Issue: A small number of units in lot number 0006573585 of the Resolute Integrity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.