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. 934 recalls have been distributed to Delaware in the last 12 months.
Showing 39761–39780 of 48,330 recalls
Recalled Item: Lotte European Waffle Recalled by Lotte International America Corp (LA...
The Issue: Lotte International is recalling the Lotte Waffles because it contains...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Stryker SmartLife Large Aseptic Housing Rx Only The Recalled by Stryker...
The Issue: The SmartLife Aseptic Housings are being recalled in that the top section of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker SmartLife Small Aseptic Housing Rx Only The Recalled by Stryker...
The Issue: The SmartLife Aseptic Housings are being recalled in that the top section of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Box Label: 3 mm Cueva Electrode Kit Recalled by Ad-Tech Medical Instrument...
The Issue: The recall has been initiated due to concerns that the applicator wand may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard¿ PerFix Light Plug The Bard¿ PerFix Light Plug is Recalled by Davol,...
The Issue: The patient record peel-off label product code and size did not match the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DEXTROAMPHETAMINE SACCHARATE Recalled by Teva Pharmaceuticals USA Due to...
The Issue: Failed Impurities/Degradation Specifications: Out of specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ZEE Aspirin 325mg - 24 tablets in single dose packets Recalled by Zee...
The Issue: Incorrect/Undeclared Excipients: ZEE Medical is recalling ZEE Aspirin due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: RESTORIS PST Acetabular Straight Shell Impactors An impactor is a Recalled...
The Issue: MAKO has identified the potential that the shell impactors may be damaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RESTORIS PST Straight Shell Inserter An impactor is a reusable Recalled by...
The Issue: MAKO has identified the potential that the shell impactors may be damaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mortara Surveyor S12 and Surveyor S19 Patient Monitors. Product Usage:...
The Issue: Martara Instrument, Inc. has recently became aware of a potential safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Persona Tibial Articular Surface Inserter is a sterilizable instrument...
The Issue: Affected product did not undergo heat treatment hardening step leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RESTORIS PST Acetabular Offset Shell Impactors An impactor is a Recalled by...
The Issue: MAKO has identified the potential that the shell impactors may be damaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accusorb MRI MAC7008 Part Number: MRI-08 MRI-Boot Product Usage: Radio...
The Issue: When not used correctly, Accusorb MRI products may overheat and lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laksell Gamma Knife Perfexion Recalled by Elekta, Inc. Due to Elekta has...
The Issue: Elekta has become aware that the latches may be locked before they have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accusorb MRI MAC7002 Part Number: MRI-02 MRI-Arm Sleeve Various Sizes...
The Issue: When not used correctly, Accusorb MRI products may overheat and lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accusorb MRI MAC7030 Product Usage: Radio frequency shielding blankets and...
The Issue: When not used correctly, Accusorb MRI products may overheat and lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HomeChoice Automated PD system and HomeChoice Pro Automated PD system...
The Issue: There are additional and updated warning and cautions that are not in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur BNP Assay for in vitro diagnostic use in Recalled by Siemens...
The Issue: Siemens Healthcare Diagnostics has confirmed that approximately 2000...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Inflation System (03.804.4135) Product Usage: Inflation system is...
The Issue: Additional instructions for use due to inability to raise the pressure above...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accusorb MRI MAC7001 Part Number: MRI-01 MRI-Large Blanket Various Sizes...
The Issue: When not used correctly, Accusorb MRI products may overheat and lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.