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. 2,491 recalls have been distributed to Arkansas in the last 12 months.
Showing 19601–19620 of 28,355 recalls
Recalled Item: Zyno Medical Administration Set Recalled by Zyno Medical LLC Due to...
The Issue: Administration Set potential filter leaking
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile IV Start Kits 50 units/trays per case Convenience kit Recalled by B....
The Issue: Positive results from non-routine sterility testing commissioned by B. Braun...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zyno Medical Administration Set Recalled by Zyno Medical LLC Due to...
The Issue: Administration Set potential filter leaking
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zyno Medical Administration Set Sterile. Rx For Use with Zyno Recalled by...
The Issue: Administration Set potential filter leaking
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zyno Medical Administration Set Recalled by Zyno Medical LLC Due to...
The Issue: Administration Set potential filter leaking
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products TSH Reagent Pack Recalled by ORTHO-CLINICAL...
The Issue: A field correction was issued by the firm for VITROS TSH reagent lot 5040...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.5mm Bowed Locking Compression Femur Plates Recalled by OrthoPediatrics...
The Issue: OrthoPediatrics Corp.is voluntarily recalling multiple lots of the 3.5mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.5mm Bowed Locking Compression Femur Plates Recalled by OrthoPediatrics...
The Issue: OrthoPediatrics Corp.is voluntarily recalling multiple lots of the 3.5mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARESCAPE VC150 Vital Signs Monitor Recalled by INNOKAS MEDICAL OY Due to A...
The Issue: A software error on released software versions 1.6.12, 1.6.12F and 1.6.16...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobalt HV Bone Cement Product Usage: Cobalt HV Bone Cement Recalled by...
The Issue: The outer packaging was mislabeled on the box indicating "Cobalt HV with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTISTE Recalled by Siemens Medical Solutions USA, Inc Due to Software patch...
The Issue: Software patch installation to address several safety issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Patient Monitor Product Usage: The monitors are indicated for...
The Issue: If an affected Patient Monitor has been powered on continuously for several...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AccuLIF PL 6-9mm x 11mm x 27mm x 8 Cage Recalled by Howmedica Osteonics...
The Issue: Since Stryker acquired the AccuLIF product in March of 2014, there have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AccuLIF PL 8-12mm x 11mm x 27mm x 8 Cage Recalled by Howmedica Osteonics...
The Issue: Since Stryker acquired the AccuLIF product in March of 2014, there have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo RT Therapist Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Software patch installation to address several safety issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AccuLIF PL 10-16mm x 11mm x 27mm x 8 Cage Recalled by Howmedica Osteonics...
The Issue: Since Stryker acquired the AccuLIF product in March of 2014, there have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRIMUS Recalled by Siemens Medical Solutions USA, Inc Due to Software patch...
The Issue: Software patch installation to address several safety issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hydroflex ELISA The HYDROFLEX is a plate washer for 96-well Recalled by...
The Issue: The batteries have the potential to overheating, melt or char.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinite F50 instrument. The INFINITE F50 instrument is a 96-well Recalled...
The Issue: The batteries have the potential to overheating, melt or char.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Custom Cardiovascular System Cardiovascular Procedure Kits labeled...
The Issue: Terumo Custom Cardiovascular Procedure Kits are labeled as Xcoating surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.