Product Recalls in Delaware
Product recalls affecting Delaware — including food, drugs, consumer products, medical devices, and vehicles distributed to Delaware. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,495 recalls have been distributed to Delaware in the last 12 months.
Showing 20561–20580 of 27,373 recalls
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: 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: 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: 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: 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: BRIELLE ORTHO CONTENDER POST-OP-KNEE BRACE LITE Model: 75-7500-087...
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: ORTHO SPEC GRP CONTENDER POST-OP-KNEE BRACE LITE Model: 75-7500-075...
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: ADV ORTHO CONTENDER POST-OP-KNEE BRACE LITE Model: 75-7500-231...
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: HAILEY ORTHO CONTENDER POST-OP-KNEE BRACE Model : 75-7500-038 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.
Recalled Item: Digital Temple Thermometer labeled under: Bestmed Recalled by Bestmed, LLC...
The Issue: An incorrect calibration of the thermometer that causes the device to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Acute Care BHCG CalPak-in vitro diagnostic product intended to...
The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Acute Care" CCRP TestPak-in vitro diagnostic product intended to...
The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Acute Care CKMB DilPak- an in vitro diagnostic product Recalled by...
The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Acute Care DDMR TestPak Catalog Number: CDDMRE SMN: 10701511...
The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Acute Care MYO DilPak Catalog Number: CMYO-D SMN:10445081 in...
The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Acute Care" MYO TestPak-in vitro diagnostic test for the Recalled by...
The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.