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. 977 recalls have been distributed to Delaware in the last 12 months.
Showing 25981–26000 of 48,330 recalls
Recalled Item: Tosoh ST AIA-PACK HbA1c Pretreatment Solution Recalled by Tosoh Bioscience...
The Issue: The assay can potentially generate erroneously elevated or erroneously...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flex Arm Product Usage: The Synthes Flex Arm is a Recalled by Synthes, Inc....
The Issue: Quick connect feature of instruments may be unable to connect to the male...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Morphine Sulfate USP Milled Recalled by Johnson Matthey Inc. Due to...
The Issue: Microbial Contamination of Non-Sterile Products: Bioburden out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lupin Hydrocodone Bitartrate and Homatropine Methylbromide Tablets Recalled...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: methylPREDNISolone Sodium Succinate for Injection Recalled by Sagent...
The Issue: Failed Impurities/Degradation Specifications: High out of specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: methylPREDNISolone Sodium Succinate for Injection Recalled by Sagent...
The Issue: Failed Impurities/Degradation Specifications: High out of specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: methylPREDNISolone Sodium Succinate for Injection Recalled by Sagent...
The Issue: Failed Impurities/Degradation Specifications: High out of specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Decitabine for Injection Recalled by InvaGen Pharmaceuticals, Inc. Due to...
The Issue: Failed impurities/degradation specifications: Failure to water content and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Flucanazole Injection Recalled by Renaissance Lakewood, LLC Due to...
The Issue: Superpotent and Failed Stability Specifications; out of specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Getinge AGS Recalled by Getinge Disinfection Ab Due to There is potential...
The Issue: There is potential for a cart with disinfected goods to unload without the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lipase Recalled by Randox Laboratories Ltd. Due to Randox has now released...
The Issue: Randox has now released further steps to avoid contamination of the Lipase...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BECKMAN COULTER iChemVELOCITY Recalled by Beckman Coulter Inc. Due to...
The Issue: Beckman Coulter has determined that there is a potential for incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Getinge AGS Recalled by Getinge Disinfection Ab Due to There is potential...
The Issue: There is potential for a cart with disinfected goods to unload without the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fabius GS Premium Recalled by Draeger Medical, Inc. Due to The automatic...
The Issue: The automatic ventilation may fail if the position detection of the motor is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fabius Tiro Recalled by Draeger Medical, Inc. Due to The automatic...
The Issue: The automatic ventilation may fail if the position detection of the motor is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fabius Tiro M Recalled by Draeger Medical, Inc. Due to The automatic...
The Issue: The automatic ventilation may fail if the position detection of the motor is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fabius MRI Recalled by Draeger Medical, Inc. Due to The automatic...
The Issue: The automatic ventilation may fail if the position detection of the motor is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIDAS LH Recalled by bioMerieux, Inc. Due to Several complaints were...
The Issue: Several complaints were received for invalid calibration with low calibrator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maximum Barrier Tray Recalled by Vygon U.S.A. Due to Potential friction...
The Issue: Potential friction holes may affect the sterility of the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Biomet Comprehensive Segmental Revision System (SRS). Orthopedic...
The Issue: During assembly, an SRS Humeral Distal Body implant failed to engage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.