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. 2,623 recalls have been distributed to Delaware in the last 12 months.
Showing 12041–12060 of 27,373 recalls
Recalled Item: iTotal CR Knee Replacement System Recalled by Conformis, Inc. Due to A...
The Issue: A limited number of tibial trays were labeled with an incorrect serial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STEALTH SPRING CLIP 6mm latis (3/4 Force). REF/UDI::A1603/(01)00607915110581...
The Issue: Failure of cardiovascular clips to provide sufficient occlusion of the vessel.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STEALTH SPRING CLIP 6mm latis (1/4 Force). REF/UDI::A1602/(01)00607915110574...
The Issue: Failure of cardiovascular clips to provide sufficient occlusion of the vessel.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STEALTH SPRING CLIP 6mm latis (1/2 Force). REF/UDI::A1601/(01)00607915110567...
The Issue: Failure of cardiovascular clips to provide sufficient occlusion of the vessel.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STEALTH SPRING CLIP 6mm latis (1/4 Force). Non-Sterile Recalled by Applied...
The Issue: Failure of cardiovascular clips to provide sufficient occlusion of the vessel.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Presource Procedure Packs containing AAMI Level 3 surgical gowns Recalled by...
The Issue: The kits contained recalled surgical gowns. The gowns were manufactured at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Presource Procedure Packs containing AAMI Level 3 surgical gowns Recalled by...
The Issue: The kits contained recalled surgical gowns. The gowns were manufactured at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic CareLink 2090 Programmer. Used to interrogate and program...
The Issue: Medtronic Conexus Telemetry has been determined to contain two primary cyber...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic CareLink Encore 29901 Programmer. Used to interrogate and program...
The Issue: Medtronic Conexus Telemetry has been determined to contain two primary cyber...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LKT200 Perfusion Circuit Recalled by Organ Recovery Systems, Inc. Due to...
The Issue: Observed leakage at the sample port assembly which could potentially lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Class IV New Era medical laser device Recalled by Inova Lasers LLC Due to...
The Issue: The firm failed to comply with the applicable standards regarding Electronic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ISE Electrolyte (2 X 2L) Reagent Recalled by Beckman Coulter Inc. Due to...
The Issue: Electrolyte reagent, used for clinical laboratory testing to determine CO2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Honeywell Pressure Transducer- Part Number: 370506-22. It is a component...
The Issue: The firm is replacing pressure transducers with an improved design due to an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JOURNEY II UNI RESECTION PREP TRIAL Recalled by Smith & Nephew, Inc. Due to...
The Issue: The spike rail was manufactured with an oversized thru-hole which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JOURNEY II UNI RESECTION PREP TRIAL Recalled by Smith & Nephew, Inc. Due to...
The Issue: The spike rail was manufactured with an oversized thru-hole which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pedicle Screws Recalled by Medicrea International Due to An internal...
The Issue: An internal component was assembled in the incorrect orientation, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QIAGEN Rotor Gene Q Software version 2.3.4. Real-time PCR analyzer Recalled...
The Issue: When using the Rotor-Gene Q with Software version 2.3.4 completing a LIMs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Iliac Screws Recalled by Medicrea International Due to An internal component...
The Issue: An internal component was assembled in the incorrect orientation, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McGRATH X3 Disposable Laryngoscope Blades-used with the McGRATH MAC Video...
The Issue: Blades do not fit the McGRATH MAC video laryngoscope handle or were tight...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protective Cover Vivo 55/65 (Used for Vivo 50/65) Recalled by Breas Medical,...
The Issue: The outlet hole of the exhalation valve control pressure tube on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.