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. 2,495 recalls have been distributed to Delaware in the last 12 months.
Showing 20581–20600 of 27,373 recalls
Recalled Item: Siemens Acute Care pBNP TestPak- in vitro diagnostic test for Recalled by...
The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Acute Care CCRP CalPak-in vitro diagnostic product intended to...
The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Acute Care CKMB TestPak- in vitro diagnostic test for Recalled by...
The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Acute Care BHCG TestPak-an in vitro diagnostic product intended...
The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Acute Care CTNI TestPak-in vitro diagnostic test for the Recalled by...
The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nebulizer Masks Opti-Mist and Opti-Mist Clear Nebulizer masks are intended...
The Issue: The Nebulizer mask malfunctions in that there is reduced or no aerosol...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexible Screw Driver SJ706R Recalled by Aesculap, Inc. Due to The flexible...
The Issue: The flexible shaft of the instruments may break during orthopedic spinal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare DuraDiagnost stationary X-ray system Recalled by Philips...
The Issue: The detector may signal that it is ready for acquisition when it actually is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniAxial Pedicle Screw & UniAxial Reduction Pedicle Screw The Response...
The Issue: Response Spine UniAxial Pedicle & UniAxial Reduction Pedicle Screws may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reagent Management System (RMS) Dimension EXL with LM Product Usage:...
The Issue: Siemens has identified RMS compressors that are missing the safety cover on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arctic Sun 5000 and Arctic Sun 2000 Recalled by C.R. Bard, Inc. Due to...
The Issue: Improper targeted temperature therapy was delivered to patients because the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexible Bone Awl Recalled by Aesculap, Inc. Due to The flexible shaft of...
The Issue: The flexible shaft of the instruments may break during orthopedic spinal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reagent Management System (RMS) Dimension EXL with LM STM Product Recalled...
The Issue: Siemens has identified RMS compressors that are missing the safety cover on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare DigitalDiagnost stationary X-ray system Recalled by...
The Issue: The detector may signal that it is ready for acquisition when it actually is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexible Drill Recalled by Aesculap, Inc. Due to The flexible shaft of the...
The Issue: The flexible shaft of the instruments may break during orthopedic spinal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reagent Management System (RMS) Dimension RxL Max HM STM Product Recalled by...
The Issue: Siemens has identified RMS compressors that are missing the safety cover on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reagent Management System (RMS) Dimension RxL Max w/o HM Product Recalled by...
The Issue: Siemens has identified RMS compressors that are missing the safety cover on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tray Set containing multiple instruments and may contain the flexible bone...
The Issue: The flexible shaft of the instruments may break during orthopedic spinal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic InSync III Recalled by Medtronic Inc. Due to Medtronic has...
The Issue: Medtronic has confirmed an issue with InSync III CRT-pacemaker devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remote Patient Monitoring System Recalled by Vidco, Inc. Due to Testing at...
The Issue: Testing at customer site showed unit Remote Patient Monitoring System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.