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. 2,586 recalls have been distributed to Delaware in the last 12 months.
Showing 14441–14460 of 27,373 recalls
Recalled Item: The Spirit Select Bed Recalled by Stryker Medical Division of Stryker...
The Issue: The beds with the high rail side rail option may not be complaint with IEC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE HEALTHCARE CARESCAPE R860 Inspiratory Safety Guard Recalled by GE...
The Issue: The ventilator Inspiratory Safety Guard (ISG) may disconnect from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIA-900 Automated Immunoassay Analyzer Recalled by Tosoh Bioscience Inc Due...
The Issue: Tosoh Bioscience has become aware of a potential issue with the axis base of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemoglobin A1c Control Recalled by Tosoh Bioscience Inc Due to Tosoh...
The Issue: Tosoh Bioscience has become aware of potential degradation of HbA1c control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Parietex Composite Parastomal Mesh (Product Number PCOPM15 / PCOPM20)...
The Issue: The firm is issuing this voluntary removal following receipt of reports of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIA-900 Analyzer Recalled by Tosoh Bioscience Inc Due to Tosoh Bioscience...
The Issue: Tosoh Bioscience has become aware of a potential issue with the pickup arm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Giraffe Omnibed - Product Usage: The OmniBed is a combination Recalled by...
The Issue: GE Healthcare has become aware of a potential safety issue that can occur if...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic MiniMed 630G 6025805-003_C Recalled by Medtronic Inc. Due to...
The Issue: Reports of occurrences in which insulin pumps with version 4.10 software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Architect system Product Usage: The Signa Architect system is Recalled...
The Issue: A small area on the bore surface, which is normally accessible to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thermacare Muscle Pain Therapy HeatWraps: a) b) Recalled by Pfizer Inc. Due...
The Issue: The firm received complaints of the wrap coming apart and leaking granular...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thermacare HeatWraps Menstrual a) b) Product Recalled by Pfizer Inc. Due to...
The Issue: The firm received complaints of the wrap coming apart and leaking granular...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neodent¿ GM Mini Conical Abutment - Product Usage: Mini Conical Recalled by...
The Issue: Laser engraved label does not match with the item in the package
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail 130 Deg 12x165mm Recalled by Zimmer Biomet, Inc....
The Issue: The set screw is not able to advance or reverse from the original position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Left Deg 9x300mm Recalled by Zimmer Biomet, Inc....
The Issue: The set screw is not able to advance or reverse from the original position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail 125 Deg 10x165mm Recalled by Zimmer Biomet, Inc....
The Issue: The set screw is not able to advance or reverse from the original position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Left 125 Deg 11x300mm Recalled by Zimmer Biomet,...
The Issue: The set screw is not able to advance or reverse from the original position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Left 125 Deg 9x165mm Recalled by Zimmer Biomet,...
The Issue: The set screw is not able to advance or reverse from the original position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Left 130 Deg 11x300mm Recalled by Zimmer Biomet,...
The Issue: The set screw is not able to advance or reverse from the original position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AF 550 x 5ML/HR CPNB Recalled by Arrow International Inc Due to Possible...
The Issue: Possible cracks on the body of the fill port connector, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AF 550 x 5ML/H FH DL 30hole SAT C Recalled by Arrow International Inc Due to...
The Issue: Possible cracks on the body of the fill port connector, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.