Product Recalls in Arkansas
Product recalls affecting Arkansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Arkansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,921 recalls have been distributed to Arkansas in the last 12 months.
Showing 21781–21800 of 49,990 recalls
Recalled Item: CYANCOBALAMIN 1200MCG/ML MDV INJECTION Recalled by RXQ Compounding LLC Due...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PHENYLEPHRINE HCL 100 MCG/ML IN NACL 0.9% 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: GLUTATHIONE 200MG/ML (PFV) INJECTION SOLN 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: ONDANSETRON 2 MG/ML INJECTION SOLUTION (NPF) 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: 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: 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.