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. 975 recalls have been distributed to Arkansas in the last 12 months.
Showing 32741–32760 of 49,990 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: 1) Ground Tumeric item #73535 Net Wt 50 lbs Distributed by Gel Spice Co....
The Issue: Ground Turmeric may contain excess levels of lead.
Recommended Action: Do not consume. Return to store for a refund or discard.
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: Desoximetasone Gel USP Recalled by Akorn, Inc. Due to Failed...
The Issue: Failed impurities/degradation specifications: product was out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or 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: la Torre Copito Marshmallow Chocolate Cookie NET WT 4.94 oz Recalled by La...
The Issue: Calcium caseinate is declared on the label, but milk is not listed.
Recommended Action: Do not consume. Return to store for a refund or discard.
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: 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: 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: 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: 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: 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: 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: 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: DRI Salicylate Serum Tox Assay Recalled by Microgenics Corporation Due to...
The Issue: Some lots of DRI Salicylate Serum Tox Assay negative patient samples are...
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.
Recalled Item: SUNRISE instrument. The INFINITE F50 instrument is a 96-well absorbance...
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: Tecan Infinite M1000 PRO The Tecan Infinite M1000 PRO is Recalled by Tecan...
The Issue: The batteries have the potential to overheating, melt or char.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.