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. 2,404 recalls have been distributed to Wyoming in the last 12 months.
Showing 21521–21540 of 48,219 recalls
Recalled Item: TRIPLE LUMEN CVC 20CM BUNDLE STCVC2040 Recalled by Centurion Medical...
The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAP CHANGE KIT DYNDC1496B Recalled by Centurion Medical Products Corporation...
The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CVC BUNDLE Recalled by Centurion Medical Products Corporation Due to Firm...
The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IV KIT - SORBAVIEW IVS3475 Recalled by Centurion Medical Products...
The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CVC BUNDLE WITHOUT CATH CVI4600 Recalled by Centurion Medical Products...
The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CENTRAL LINE BUNDLE ECVC6375 Recalled by Centurion Medical Products...
The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PORT AND IO ACCESS DRESSING KIT DT15780A Recalled by Centurion Medical...
The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lemon balm leaf c/s Recalled by AmeriHerb International Inc Due to Potential...
The Issue: Dried spice and herb products potentially contaminated with generic E. coli.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Parsley flakes Recalled by AmeriHerb International Inc Due to Potential E....
The Issue: Dried spice and herb products potentially contaminated with generic E. coli.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Goldenseal herb c/s Recalled by AmeriHerb International Inc Due to Potential...
The Issue: Dried spice and herb products potentially contaminated with generic E. coli.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Dill weed c/s Recalled by AmeriHerb International Inc Due to Potential E....
The Issue: Dried spice and herb products potentially contaminated with generic E. coli.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Blessed thistle herb c/s Recalled by AmeriHerb International Inc Due to...
The Issue: Dried spice and herb products potentially contaminated with generic E. coli.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Mullein leaf c/s Recalled by AmeriHerb International Inc Due to Potential E....
The Issue: Dried spice and herb products potentially contaminated with generic E. coli.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: DIVALPROEX SODIUM EXTENDED-RELEASE TABLETS Recalled by MAJOR PHARMACEUTICALS...
The Issue: cGMP deviations: Product was exposed above 50% relative humidity levels...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium Tablets USP 50 mg 50 tablets (5x10) Unit Recalled by...
The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium Tablets USP 25 mg 50 tablets (5x10) Unit Recalled by...
The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl Citrate Injection Recalled by Akorn Inc Due to Failed...
The Issue: Failed impurities/degradation specification: Out of Specification result for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Titanium 4000 Recalled by D.B.P. Distribution Due to Undeclared Sildenafil
The Issue: Marketed without an approved NDA/ANDA: undeclared sildenafil and tadalafil.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Arrow¿ JACC with Chlorag+ard Technology Product Code: JR 42541 HPHNM...
The Issue: Lidstock states the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Connected OR Cart Recalled by Stryker Corporation Due to There is a...
The Issue: There is a potential problem with firm s Connected OR Cart, 120V resulting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.