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. 2,559 recalls have been distributed to Delaware in the last 12 months.
Showing 18021–18040 of 27,373 recalls
Recalled Item: Philips Healthcare Brilliance 64 System Recalled by Philips Electronics...
The Issue: During a bolus tracking procedure, no images were generated when the scan...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare Brilliance iCT X-Ray Recalled by Philips Electronics...
The Issue: During a bolus tracking procedure, no images were generated when the scan...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare Brilliance iCT SP X-Ray Recalled by Philips Electronics...
The Issue: During a bolus tracking procedure, no images were generated when the scan...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare Ingenuity Core128 X-Ray Recalled by Philips Electronics...
The Issue: During a bolus tracking procedure, no images were generated when the scan...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Video Duodenoscope These instruments are intended to provide optical...
The Issue: Pentax initiated a field correction/safety alert for two (2) models of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Strata II / Strata NSC Valves (includes Burr Hole Recalled by...
The Issue: Medtronic Neurosurgery initiated a recall after receiving five (5) Product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 12 Defibrillator/Monitor with End-Tidal CO2 option. The device is...
The Issue: The End-Tidal CO2 (EtCO2) reading can intermittently show a value of XXX...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 15 Monitor/Defibrillator with End-Tidal CO2 option. Intended for use...
The Issue: The End-Tidal CO2 (EtCO2) reading can intermittently show a value of XXX...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer Buffered Sodium Citrate: (9NC) Blood Collection Tube (4.5...
The Issue: A portion of this lot of blood collection tubes was manufactured with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The LIFEPAK 1000 defibrillator is intended for use by personnel Recalled by...
The Issue: The firm has received complaints that the LIFEPAK 1000 Defibrillator is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Teleflex Green Non-Latex Robertazzi Nasopharyngeal Airway Recalled by...
The Issue: Labeling error
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compressible Limb Therapy System (Leg Cuffs Recalled by Won Industry Co. Due...
The Issue: Distribution of unapproved devices with incorrect air compression level setup
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Morning Life Recalled by Won Industry Co. Due to Distribution of unapproved...
The Issue: Distribution of unapproved devices with incorrect air compression level setup
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Recalled by Boston Scientific Corporation Due to There is...
The Issue: There is a potential for radio frequency (RF) interference to alter wireless...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GrebSet Micro-Introducer Kit Recalled by Vascular Solutions, Inc. Due to...
The Issue: Four Lots of GrebSet Micro-introducer Kits, model 7941, contain guidewires...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 15 Monitor Recalled by Physio-Control, Inc. Due to The firm has...
The Issue: The firm has become aware of a potential device issue where the LIFEPAK 15...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carestream DRX-Revolution Mobile X-Ray System Recalled by Carestream Health...
The Issue: The firm received a complaint alleging that a DRX Revolution System could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mammomat Inspiration full Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: Software error
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: N Latex HCY REAGENT Recalled by Siemens Healthcare Diagnostics, Inc. Due to...
The Issue: The firm confirmed a reduced once-opened and on-board stability for N Latex...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vascular catheter introduction kit The PICC is indicated for short Recalled...
The Issue: There have been complaints for peel away sheaths flaring
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.