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. 2,478 recalls have been distributed to Arkansas in the last 12 months.
Showing 21341–21360 of 28,355 recalls
Recalled Item: ProScreen 8 Panel Dip Card Recalled by Ameditech Inc Due to Ameditechs Drugs...
The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProScreen 8 Panel Dip Card w/Adult Recalled by Ameditech Inc Due to...
The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Immutest Cup CLIA Waived w/Adulteration Recalled by Ameditech Inc Due to...
The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DrugSmart 10 Test Cup (PCP & OXY) Recalled by Ameditech Inc Due to...
The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DrugSmart Dip AMP/OPI2/COC/THC/BZO Test Recalled by Ameditech Inc Due to...
The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProScreen 6 Panel Dip Card w/Adult (AU) Recalled by Ameditech Inc Due to...
The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProScreen 12 Panel Dip Card Recalled by Ameditech Inc Due to Ameditechs...
The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ImmuTest 12 Panel Dip Card Recalled by Ameditech Inc Due to Ameditechs Drugs...
The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProScreen CLIA Wvd 12 Panel Cup w/Adult. Recalled by Ameditech Inc Due to...
The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaPACS Diagnostic Viewer versions 8.3.7 Recalled by Novarad Corporation...
The Issue: The SUV values that are being calculated in the PET/CT fusion tool are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProScreen 6 Panel Cassette w/Adult (AU) Recalled by Ameditech Inc Due to...
The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RealityCHECK Tilt Cup 12 Panel + Adult Recalled by Ameditech Inc Due to...
The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iCup DX 11 Panel w/ Adulterant Recalled by Ameditech Inc Due to Ameditechs...
The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Recalled by STERILMED, INC. Due to Sterilmed, Inc. is voluntarily...
The Issue: Sterilmed, Inc. is voluntarily recalling all unexpired Reprocessed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima IGS 320. Product Usage: The angiographic X-ray Recalled...
The Issue: GE Healthcare has recently become aware of a potential safety issue related...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet HCU 30 Coolant Type R134A Filling weight 250 g Recalled by Maquet...
The Issue: Failure of the HEATER-COOLER UNIT (HCU 30) Type 2 power supply board. A drop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima CL323i Product Usage: The angiographic X-ray systems...
The Issue: GE Healthcare has recently become aware of a potential safety issue related...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CONTENDER POST-OP-KNEE BRACE FULL FOAM Model: 75-7550-000 Post-Operative...
The Issue: Knee brace could fail to maintain the locked position and a loss of balance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CT ORTHO CONTENDER POST-OP-KNEE BRACE LITE Model: 75-7500-011 Post-Operative...
The Issue: Knee brace could fail to maintain the locked position and a loss of balance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corflex Contender Post-Op Knee Brace Lite Model: 75-7500-000 Post-Operative...
The Issue: Knee brace could fail to maintain the locked position and a loss of balance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.