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. 2,457 recalls have been distributed to Delaware in the last 12 months.
Showing 25881–25900 of 27,373 recalls
Recalled Item: Surgical microscope The device is used to improve the visibility Recalled by...
The Issue: The brake in the Z axis and/or brakes in the AB and C axes failed during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Needle Counters with Blade Disarmer Recalled by Cardinal Health Due to Small...
The Issue: Small holes (approximately 1 mm or less) found in device unit level...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Needle Counters with Blade Disarmer Recalled by Cardinal Health Due to Small...
The Issue: Small holes (approximately 1 mm or less) found in device unit level...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Surgical Bed Recalled by Stryker Medical Division of Stryker...
The Issue: Stryker Medical Model 3002S3EX and Model 3005S3EX beds built between March...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mizuho Orthopedic Table Recalled by Mizuho OSI Due to Possible instability...
The Issue: Possible instability of Orthopedic Table Top. If the epoxy bond fails, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Animas(R) 2020 Recalled by Animas Corporation Due to Due to an internal...
The Issue: Due to an internal calendar date limit (December 31, 2015) these pumps will...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medacta Quadra Trial Broach size 0 part # 01.10.10.045 Recalled by Medacta...
The Issue: The tip of the Quadra Trial Broach size 0, broke during a surgery.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QuietCare-Networked product Recalled by Intel-GE Care Innovations LLC Due to...
The Issue: Care Innovations detected a software anomaly: During the engineering...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ortho Clinical Diagnostics VITROS¿ Chemistry Products Vapor Adsorption...
The Issue: Some VITROS¿ Chemistry Products Vapor Adsorption Cartridge CAT No. 6800100...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Medical Components, Inc dba MedComp Due to The affected product...
The Issue: The affected product was packaged with the incorrect introducer needle. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SR Instruments FG3105 Patient Scales Used on various Joerns Healthcare...
The Issue: SR Instruments Inc. is implementing a field correction for the Joerns...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Juno DRF Recalled by Philips Healthcare Inc. Due to Values of fluoroscopy...
The Issue: Values of fluoroscopy time, Air Kerma Rate and Cumulated Air Kerma may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Laboratories Recalled by Abbott Laboratories Due to The Architect...
The Issue: The Architect 25-OH Vitamin D assay has the potential to generate falsely...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aplio 500/400/300 Diagnostic Ultrasound System (TUS-500/400/300). Device...
The Issue: Toshiba Medical Systems has received reports of startup issues with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BBL(TM) Fildes Enrichment Recalled by Becton Dickinson & Co. Due to...
The Issue: Enrichment media intended to enhance the cultivation of various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flowtron Trio DVT Pump Recalled by Arjo, Inc. dba ArjoHuntleigh Due to The...
The Issue: The Flowtron Trio DVT Pump has been marketed without proper FDA Approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Emit(R) tox(TM) Serum Calibrators Recalled by Siemens Healthcare...
The Issue: Incorrect expiration date was assigned to the D1 lot of Emit(R) tox(TM)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liko Standard Slingbar 450. The Standard Slingbar 450 is a Recalled by...
The Issue: Liko/Hill-Rom has received reports from facilities which indicate that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Companion External Battery Recalled by SynCardia Systems Inc. Due to...
The Issue: Syncardia Systems is recalling the Companion External Batteries used with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Canon Full Auto RK-F2 Recalled by Canon Inc. Due to Canon Inc. had received...
The Issue: Canon Inc. had received 17 claims from our foreign sales companies between...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.