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 21341–21360 of 27,373 recalls
Recalled Item: Spine Wave Access Kit Recalled by Spine Wave, Inc. Due to Mislabeling
The Issue: Mislabeled outer carton: Monopolar Probe is listed as 200 x 1.5mm when it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Navigation System II-Cart Recalled by Stryker Instruments Div. of Stryker...
The Issue: Stryker initiated a device recall of the Navigation System II-Cart, Camera...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synovis VASCU-GUARD Peripheral Vascular Patch in the following sizes and...
The Issue: Baxter healthcare is recalling specific product codes of Vascu-Guard...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI Custom Eyes¿ Ophthalmic Procedure Kits with the component -Devon...
The Issue: Devon Light Glove in procedure kits may have holes/slits compromising...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI Custom Eyes¿ Ophthalmic Procedure Kits with the component -Devon...
The Issue: Devon Light Glove in procedure kits may have holes/slits compromising...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI Custom Eyes¿ Ophthalmic Procedure Kits with the component -Devon...
The Issue: Devon Light Glove in procedure kits may have holes/slits compromising...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra¿ Long Epidural Steroid Injection Needle (Tuohy Needle) Recalled by...
The Issue: Integra LifeSciences Corp. d.b.a. Integra Pain Management Announces...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI Custom Eyes¿ Ophthalmic Procedure Kits with the component -Devon...
The Issue: Devon Light Glove in procedure kits may have holes/slits compromising...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI Custom Eyes¿ Ophthalmic Procedure Kits with the component -Devon...
The Issue: Devon Light Glove in procedure kits may have holes/slits compromising...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Unilateral external fixation ankle clamp Product Usage: Unilateral external...
The Issue: Ankle clamp was assembled incorrectly; the offset of the pin to the pivot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Base for Terumo Advanced Perfusion System 1 Recalled by Terumo...
The Issue: Terumo CVS is implementing field correction activities to address the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 100/120V AC Recalled by Terumo Cardiovascular Systems Corporation Due to...
The Issue: Terumo CVS is implementing field correction activities to address the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ULTRA-FAST FIX Knot Pusher Suture Cutters Product Number: 72201537 Intended...
The Issue: Sterility of device maybe compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: I-Portal¿ NOTC and VNG Recalled by Neuro Kinetics, Inc. Due to complaints of...
The Issue: complaints of system malfunction and unintended, sudden movement at start...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRI Femoral Impactor Block for knee prosthesis surgery. Orthopedic Manual...
The Issue: Potential for uncured adhesive between the metal threaded insert and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cortical Screw for M/DN Intramedullary Fixation. Metaphyseal/Diaphyseal Nail...
The Issue: The entire scope of 4.5mm Cortical Screws listed as compatible with the M/DN...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare Ventricular Assist System (HVAD) For use as a bridge-to-cardiac...
The Issue: Complaints with the HVAD Abnormal Power Source Switching.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare Ventricular Assist System (HVAD). Catalog #'s US: 1101 and...
The Issue: HeartWare has received complaints relating to damage or bent connection pins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EasyLink Data Management System Recalled by Siemens Healthcare Diagnostics,...
The Issue: System Limitations and Software Issues related to the following features:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare Ventricular Assist System (HVAD). Catalog #'s US: 1101 and...
The Issue: Complaints with the HVAD Internal Controller Alarm Battery failures.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.