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 20981–21000 of 48,219 recalls
Recalled Item: NEOSTIGMINE METHYL SULFATE 1MG/ML INJ SOL SYR Recalled by RXQ Compounding...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EDETATE CALCIUM DISODIUM 150MG/ML INJECTABLE Recalled by RXQ Compounding LLC...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: WOODSTOCK ORGANIC GRILLED RED PEPPER Recalled by UNFI General Corporate Due...
The Issue: Product tested positive for Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sterile Co-Flex Med 4" - Product Usage: Single Use secondary Recalled by...
The Issue: Incomplete packaging seal of sterile product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Co-Flex NL 3" - Product Usage: Single Use secondary Recalled by...
The Issue: Incomplete packaging seal of sterile product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Co-Flex LF2 3" - Product Usage: Single Use secondary Recalled by...
The Issue: Incomplete packaging seal of sterile product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Co-Flex Med 3" - Product Usage: Single Use secondary Recalled by...
The Issue: Incomplete packaging seal of sterile product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Co-Flex LF2 4" - Product Usage: Single Use secondary Recalled by...
The Issue: Incomplete packaging seal of sterile product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Co-Flex NL 4" - Product Usage: Single Use secondary Recalled by...
The Issue: Incomplete packaging seal of sterile product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iGUIDE System with software build iGuide 2.2.0 Recalled by Elekta, Inc. Due...
The Issue: Potential for iGUIDE to incorrectly monitor the 3D position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ElectroMist product codes: 36-3310-25 - Product Usage: Electrode...
The Issue: Potential for failed stability antimicrobial effectiveness testing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alpha Conducting solution product codes: 3310-25 ASCR - Product Usage:...
The Issue: Potential for failed stability antimicrobial effectiveness testing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ElectroMist product codes: 36-3310-60 - Product Usage: Electrode...
The Issue: Potential for failed stability antimicrobial effectiveness testing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ElectroMist product codes: 36-3310-04 - Product Usage: Electrode...
The Issue: Potential for failed stability antimicrobial effectiveness testing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alpha Conducting solution product codes:3310-15 ACS - Product Usage:...
The Issue: Potential for failed stability antimicrobial effectiveness testing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Droperidol Injectable Sterile Solution Recalled by Premier Pharmacy Labs Inc...
The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brilliant Blue Ophthalmic PF INJ Recalled by Premier Pharmacy Labs Inc Due...
The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Neostigmine Methylsulfate Recalled by Premier Pharmacy Labs Inc Due to Lack...
The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SUCCINYLcholine Chloride Recalled by Premier Pharmacy Labs Inc Due to Lack...
The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SUCCINYLcholine Chloride Recalled by Premier Pharmacy Labs Inc Due to Lack...
The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.