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. 2,367 recalls have been distributed to Wyoming in the last 12 months.
Showing 26781–26800 of 48,219 recalls
Recalled Item: Berry Flavor Immune Support Dietary Supplement Effervescent Tablets 10...
The Issue: The label does not list "Sodium" in the ingredient statement.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Carl Zeiss INTRABEAM PRS 500 Recalled by Carl Zeiss Meditec AG Due to The...
The Issue: The device had an incorrect printed calibration value on the calibration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours...
The Issue: Defective Delivery System: Products no longer meet the release liner removal...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vancomycin Hydrochloride for Injection Recalled by Pfizer Inc. Due to...
The Issue: Presence of Particulate Matter: glass particulate found in vial
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Delivers 30 mg over 9 hours...
The Issue: Defective Delivery System: Products no longer meet the release liner removal...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Delivers 20 mg over 9 hours...
The Issue: Defective Delivery System: Products no longer meet the release liner removal...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Delivers 15 mg over 9 hours...
The Issue: Defective Delivery System: Products no longer meet the release liner removal...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PIYANPING Anti-Itch (hydrocortisone) Lotion Recalled by Lucky Mart Inc. Due...
The Issue: Incorrect Product Formulation: product contains dexamethasone instead of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Enalapril Maleate Tablets Recalled by Amerisource Health Services Due to...
The Issue: Failed Stability Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BD Vacutainer¿ K2 EDTA (K2E) 3.6mg Blood Collection Tube (13 Recalled by...
The Issue: A limited portion of the lot was manufactured with less than the required...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fortify VR - Model Numbers: CD1231-40 and CD1231-40Q Recalled by St Jude...
The Issue: The device may exhibit premature battery depletion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona Partial Knee System Product Usage: The Persona Partial Knee Recalled...
The Issue: Potential for the Persona Partial Knee Impactor Pad to fracture.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Unify Recalled by St Jude Medical Inc. Due to The device may exhibit...
The Issue: The device may exhibit premature battery depletion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G7 DUAL MOBILITY LINER 44MM F Product Usage: Intended for Recalled by Zimmer...
The Issue: The affected products are labeled and etched as F-44 mm liners; however, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AGC 2000 LP Patella Recalled by Zimmer Biomet, Inc. Due to The affected AGC...
The Issue: The affected AGC 2000 LP Patella products were over-molded leaving the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AGC 2000 LP Patella Recalled by Zimmer Biomet, Inc. Due to The affected AGC...
The Issue: The affected AGC 2000 LP Patella products were over-molded leaving the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AArtis Q/ Q.Zen biplane Artis zee biplane Product Usage: Artis Recalled by...
The Issue: Within a specific number of Artis zee biplane and Artis Q biplane systems, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lyophilized Chemistry Calibrator Level 1 Product Usage: Beckman Coulter...
The Issue: Unpaired lots of AU lyophilized chemistry calibrator level 1 and 2 have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.plaza systems with SW VB20A Recalled by Siemens Medical Solutions USA,...
The Issue: When a prior study is being replaced in the workflow step, in certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Multi Measurement Server Recalled by Philips Electronics North...
The Issue: Distorted ST-Segment when using 12-Lead ECG Monitoring with Philips...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.