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. 2,655 recalls have been distributed to Delaware in the last 12 months.
Showing 7101–7120 of 27,373 recalls
Recalled Item: Non-sterile procedural trays labeled as ORTHO TRAUMA Recalled by MEDLINE...
The Issue: Potential for sterile blades, within non-sterile SPT kits containing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Non-sterile procedural trays labeled as CRANI Recalled by MEDLINE...
The Issue: Potential for sterile blades, within non-sterile SPT kits containing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Non-sterile procedural trays labeled as TOTAL KNEE KIT Recalled by MEDLINE...
The Issue: Potential for sterile blades, within non-sterile SPT kits containing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Non-sterile procedural trays labeled as THEDA CLARK TOTAL KNEE CDS Recalled...
The Issue: Potential for sterile blades, within non-sterile SPT kits containing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Non-sterile procedural trays labeled as LAPAROTOMY CDS Recalled by MEDLINE...
The Issue: Potential for sterile blades, within non-sterile SPT kits containing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Non-sterile procedural trays labeled as LAPAROSCOPIC Recalled by MEDLINE...
The Issue: Potential for sterile blades, within non-sterile SPT kits containing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Intact PTH Reagent Pack- IVD For the...
The Issue: Lower than expected iPTH patient and Quality Control (QC) results, reported...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Programmable Diagnostic Computer Recalled by Siemens Medical Solutions USA,...
The Issue: The firm will be performing a software update to address a software error...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConvaTec AQUACEL Foam Ag Adhesive Recalled by ConvaTec, Inc Due to ConvaTec...
The Issue: ConvaTec are voluntarily recalling a batch of AQUACEL¿ Foam Ag Adhesive 10cm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iTotal Identity Impactor Handle Recalled by Conformis, Inc. Due to Loctite...
The Issue: Loctite thread locker (epoxy) may not have been applied to the screw that is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omnipod 5 Automated Insulin Delivery System Product catalog numbers:...
The Issue: The firm has become aware of an issue with the Omnipod 5 Controller where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Power-PRO 2 Recalled by Stryker Medical Division of Stryker Corporation Due...
The Issue: Cot may experience unintended motion due to damaged cables. Potential risk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vivid S6 ultrasound. Used in ultrasound imaging and analysis in Recalled by...
The Issue: Potential for batteries that have not been replaced at 2 years, as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vivid S5 N ultrasound. Not marketed in the US. Used Recalled by GE Medical...
The Issue: Potential for batteries that have not been replaced at 2 years, as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vivid S5 Ultrasound. Used in ultrasound imaging and analysis in Recalled by...
The Issue: Potential for batteries that have not been replaced at 2 years, as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vivid i ultrasound. Marketed under the following 510(k) numbers: K033139...
The Issue: Potential for batteries that have not been replaced at 2 years, as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vivid q ultrasound. Used in ultrasound imaging and analysis in Recalled by...
The Issue: Potential for batteries that have not been replaced at 2 years, as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vivid q N ultrasound. Not marketed in the US. Used Recalled by GE Medical...
The Issue: Potential for batteries that have not been replaced at 2 years, as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X-CORE 2 Ti Core Recalled by NuVasive Inc Due to Potential that insert will...
The Issue: Potential that insert will be unable to disengage from the vertebral body...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vivid S6 N ultrasound. Not marketed in the US. Used Recalled by GE Medical...
The Issue: Potential for batteries that have not been replaced at 2 years, as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.