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. 2,694 recalls have been distributed to Delaware in the last 12 months.
Showing 2641–2660 of 27,373 recalls
Recalled Item: BD BACTEC FX40 Instrument Version or Model: 442296 Catalog Number: 442296...
The Issue: BD confirmed that product service credentials used by some BD technical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BACTEC 9120 System Version or Model: 445570 Catalog Number: 445570 Recalled...
The Issue: BD confirmed that product service credentials used by some BD technical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix M50 Automated Microbiology System Version or Model: 443624...
The Issue: BD confirmed that product service credentials used by some BD technical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Offset Cup Impactor - 3/8-16 interface. Reusable surgical instrument used...
The Issue: Recalled lot does not meet specification and has reported incidents of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Daytona Small Stature Product Name: CoCr LockingCap 4.5mm...
The Issue: Due to manufacturing defects observed on Locking Caps that affect the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Daytona Small Stature Product Name: Ti Locking Cap 4.5mm...
The Issue: Due to manufacturing defects observed on Locking Caps that affect the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIORAPTOR Suture Anchors. Tendon/ligament Recalled by Smith & Nephew Inc....
The Issue: Sterile barrier breach due to inadequate packaging design that could not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMS Artificial Urinary Sphincter Control Pump Recalled by Boston Scientific...
The Issue: Potential for mislabeled packaging in which a device labeled as a Pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMS Artificial Urinary Sphincter Pressure Regulating Balloon 61-70 cm H2O...
The Issue: Potential for mislabeled packaging in which a device labeled as a Pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Architect AIR Recalled by GE Medical Systems, LLC Due to Gradient...
The Issue: Gradient coils for certain MR systems (see affected product list in this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery MR750w 3.0T Recalled by GE Medical Systems, LLC Due to Gradient...
The Issue: Gradient coils for certain MR systems (see affected product list in this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Architect Recalled by GE Medical Systems, LLC Due to Gradient coils...
The Issue: Gradient coils for certain MR systems (see affected product list in this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tomographic Imager Combining Emission Computed Tomography With Nuclear...
The Issue: Gradient coils for certain MR systems (see affected product list in this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tempus LS-Manual Defibrillator Model 00-3020 The Tempus LS-Manual is a...
The Issue: Due to incorrect labels applied to devices during servicing. Labels contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Galaxy bronchoscope (Product GALB-001) used with Instructions for use...
The Issue: Not all biopsy tools meant to fit bronchoscope channel (2.1mm inner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ENDO KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Identified...
The Issue: Identified lots of Olympus product may be missing sterile and manufacturing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Proteus XR/A radiographic system Recalled by GE Healthcare (China) Co.,...
The Issue: Steel cables in the Wall Stand for certain Proteus XR/a systems serviced by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICRO-X Rover Mobile X-ray System Recalled by Micro-X Ltd. Due to During...
The Issue: During internal testing it was found that if the system is Ready to expose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lab Kit Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Specimen...
The Issue: Specimen container included in kits is labeled as sterile, but has been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: URINE COLLECTION VHC Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...
The Issue: Specimen container included in kits is labeled as sterile, but has been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.