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. 2,391 recalls have been distributed to Wyoming in the last 12 months.
Showing 23761–23780 of 27,462 recalls
Recalled Item: GLOBAL¿ Anchor Peg Glenoid Plus (APG+) 2.5MM Breakaway Guide Pin Recalled by...
The Issue: Urgent Device Correction notifications are being sent to USA distributors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Henora 300psi I.V. Catheter Extension Set Product Usage: Recalled by RGI...
The Issue: Problem with low adhesion of the tubing to luer connection which may lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance CT 16 Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: Block assembly-lock stop subframe of service latch was not manufactured to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proteus 235 Proton Therapy System for cancer treatment. Recalled by Ion Beam...
The Issue: While the Proteus 235 is in the pencil beam scanning (PBS) treatment mode,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sit/stand Rolling Walker Recalled by Central Purchasing LLC DBA Harbor...
The Issue: Harbor Freight Tools intiaited a recall of Sit/Stand Rolling Walker...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Vivid E9 Ultrasound System Recalled by GE Healthcare, LLC Due to GE...
The Issue: GE Healthcare has recently become aware of a potential safety issue where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INOmax DSIR Recalled by INO Therapeutics (dba Ikaria) Due to An anomaly...
The Issue: An anomaly impacts the monitoring system of INOmax DSIR Plus (software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Osteo-Clage System consists of stainless steel cable/sleeves and...
The Issue: Manufacturing of these devices with a grade of stainless steel that is not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Specialty Diluent Recalled by Ortho-Clinical...
The Issue: Ortho Clinical Diagnostics (OCD) confirmed the potential for lower than...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Acumed Tension Band Pin is a fixation pin which Recalled by Acumed LLC...
The Issue: Certain lots of Acumed Tension Band Pins are being recalled because the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products FS Diluent Pack 3 Recalled by Ortho-Clinical...
The Issue: Ortho Clinical Diagnostics (OCD) confirmed the potential for lower than...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ToxCup Drug Screen Cup Recalled by Branan Medical Corporation Due to May be...
The Issue: May be labeled with incorrect result interpretation graphics on the ToxCup...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker PenAdapt" Recalled by Stryker Instruments Div. of Stryker...
The Issue: During packaging verification testing, a failure occurred due to cuts in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reusable latex breathing bags with multiple part numbers and sold Recalled...
The Issue: Reusable latex breathing bags with various part numbers and sold as part of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LATEX-FREE Recalled by Hospira Inc. Due to The Tyvek cover may not be...
The Issue: The Tyvek cover may not be completely sealed to the rest of the package...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur Folate Cat No. 06891541 SMN 10325366 (500 Recalled by...
The Issue: Serum controls may go out of range low with the ADVIA Centaur ¿Systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LATEX-FREE Recalled by Hospira Inc. Due to The Tyvek cover may not be...
The Issue: The Tyvek cover may not be completely sealed to the rest of the package...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AlloFuse DBM Putty 5cc Recalled by AlloSource, Inc. Due to The donor was...
The Issue: The donor was hemodiluted.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LATEX-FREE Recalled by Hospira Inc. Due to The Tyvek cover may not be...
The Issue: The Tyvek cover may not be completely sealed to the rest of the package...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LATEX-FREE Recalled by Hospira Inc. Due to The Tyvek cover may not be...
The Issue: The Tyvek cover may not be completely sealed to the rest of the package...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.