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. 2,668 recalls have been distributed to Delaware in the last 12 months.
Showing 5361–5380 of 27,373 recalls
Recalled Item: Compress Device Short Anchor Plug Recalled by Biomet, Inc. Due to Anchor...
The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compress Device Segmental Anchor Plug Recalled by Biomet, Inc. Due to Anchor...
The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compress Device Segmental Anchor Plug Recalled by Biomet, Inc. Due to Anchor...
The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compress Device Short Anchor Plug Recalled by Biomet, Inc. Due to Anchor...
The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compress Device Segmental Anchor Plug Recalled by Biomet, Inc. Due to Anchor...
The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance CT Big Bore with software version V4.8.0.10421 Model:728244 CT...
The Issue: For oncology users: If the user performed off-set reconstruction on CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Big Bore RT with software version V4.8.0.10421- Model: 728242 CT Recalled by...
The Issue: For oncology users: If the user performed off-set reconstruction on CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spectral CT on Rails Recalled by Philips North America Due to When preparing...
The Issue: When preparing for CCT Fluoroscopy mode and activating the CCT foot pedal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance CT Big Bore Oncology with software version V4.8.0.10421...
The Issue: For oncology users: If the user performed off-set reconstruction on CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MED-810A Zemits NDPrime Laser products Recalled by Advance-Esthetic LLC Due...
The Issue: Advance-Esthetic LLC failed to comply with the applicable standards...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D-Clip Standard/Mini Applier Recalled by Peter Lazic Gmbh Due to Customer...
The Issue: Customer complaint received that reported the applier failed during surgery....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D-Clip Standard/Mini Applier Recalled by Peter Lazic Gmbh Due to Customer...
The Issue: Customer complaint received that reported the applier failed during surgery....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D-Clip Standard/Mini Applier Recalled by Peter Lazic Gmbh Due to Customer...
The Issue: Customer complaint received that reported the applier failed during surgery....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORION System with software OSS v6.0 and OSS v7.0- An Recalled by LEONI CIA...
The Issue: Users of the patient positioning system ORION System can be faced with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORION System with software OSS v6.0 and OSS v7.0- An Recalled by LEONI CIA...
The Issue: Users of the patient positioning system ORION System can be faced with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDFLEX Recalled by CareFusion 303, Inc. Due to If "Clear All" selected...
The Issue: If "Clear All" selected medications is selected on patient profile, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Encore Medical, LP Due to Mislabeling
The Issue: Mislabeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reverse Shoulder System e+ Recalled by Encore Medical, LP Due to Mislabeling
The Issue: Mislabeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CereLink ICP Extension Cable (Extension Cable) Recalled by Integra...
The Issue: Firm is expanding the existing recall RES 90457 for the Cerelink, initiated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mobilett Mira wireless (VA20) mobile x-ray system(s) Recalled by Siemens...
The Issue: Due to the incorrect mounting of the buzzer component, there is no acoustic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.