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. 2,623 recalls have been distributed to Delaware in the last 12 months.
Showing 11961–11980 of 27,373 recalls
Recalled Item: Infinix-8000C with Catheterization Table CAT-850B or CAT-860B - Product...
The Issue: Bolts holding the longitudinal movement of catheterization tables may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Captus 4000e Thyroid Uptake System Recalled by Capintec Inc Due to It is...
The Issue: It is possible that the collimators have screw hole locations that were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merits E604 Pilot Navigator Stairlift - Product Usage: To transport Recalled...
The Issue: Pinion gear may disengage from track allowing lift to slip or jolt.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ReWalk Personal 6.0 Recalled by Argo Medical Technologies Ltd Due to ReWalk...
The Issue: ReWalk Robotics received two complaints (one in the US; one in the Germany),...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex Lumbar Puncture Tray. Anesthesia Conduction Kit. 4826PL-20 - Product...
The Issue: Cases of Portex¿ Lumbar Puncture Tray Child, SKU #4826PL-20 had been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merlin PCS 3650 Software Upgrade Kit Recalled by Abbott Due to Internal...
The Issue: Internal testing of software identified software anomaly scenarios where if...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: uDR 596i Digital Medical X-Ray Imaging System - Product Usage: Recalled by...
The Issue: Two issues were identified with the stationary x-ray system. 1. Some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH 930 Analyzer Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: Editing an assay Test Definition and switching to another assay s Test...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentell Hydrogel Ag 4x4 Recalled by Gentell, Inc Due to During an FDA audit,...
The Issue: During an FDA audit, it was discovered that the product was not properly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentell Hydrogel Ag 4oz. Tube Recalled by Gentell, Inc Due to During an FDA...
The Issue: During an FDA audit, it was discovered that the product was not properly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAVIO Soft Tissue Protector Recalled by Smith & Nephew, Inc. Due to...
The Issue: Potential for the NAVIO Soft Tissue Protector to become stuck or bound to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentell Hydrogel Ag 2x2 Recalled by Gentell, Inc Due to During an FDA audit,...
The Issue: During an FDA audit, it was discovered that the product was not properly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentell Hydrogel Ag 4x8 Recalled by Gentell, Inc Due to During an FDA audit,...
The Issue: During an FDA audit, it was discovered that the product was not properly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The CapsoCam Plus (SV-3) Recalled by Capso Vision, Inc. Due to Ingestible...
The Issue: Ingestible video capsule system has capsule with incorrect capture mode...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartStart MRx Monitor/Defibrillators with model numbers M3535A M3536A...
The Issue: Philips has received a number of reports of HeartStart MRx...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nexus Universal with OptiBond Universal Recalled by Kerr/Pentron, DBA Kerr...
The Issue: An issue within production process used to package trial kits let to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Butterfly iQ Ultrasound System Auto Bladder Volume Tool-The Auto Bladder...
The Issue: Distributed without an approved 510(k)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Butterfly iQ Ultrasound System containing the Auto EF(Ejection Fraction)...
The Issue: Distributed without an approved 510(k)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LivaNova Heater-Cooler System 3T - Product Usage: The Heater-Cooler 3T...
The Issue: The firm is providing validated cleaning and disinfection instructions in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: R-F Injector Cannula. 18gx10cm-STERILE. REF/UDI: 257-1810/(01)00828788021496...
The Issue: Incorrect expiration date on introduction cannula packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.