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 21141–21160 of 27,373 recalls
Recalled Item: GE Healthcare Precision 500D Classical R & F system. Recalled by GE...
The Issue: A reported incident of a monitor that fell from the suspension. A fall of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ASP-1021 LipoTower with Aspiration Pump and Tumescent Pump. Medical use....
The Issue: There is potential risk of electrical shock if lead wires inside the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Etest Cefotaxime CT 256 WW and Etest Cefotaxime CT 256 US. in vitro...
The Issue: QC results were out of range resulting in false resistant strains.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE CONV RP CR ARTICULATION SURFACE SZ1 Recalled by DePuy Orthopaedics,...
The Issue: Potential for the Balseal, a small wire spring coil located on the post...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ASP-1020 LipoTower with Aspiration Pump. Medical use. Recalled by MicroAire...
The Issue: There is potential risk of electrical shock if lead wires inside the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE CONV FB PS ARTICULATION SURFACE SZ1-10 INTENDED USE: The Recalled by...
The Issue: Potential for the Balseal, a small wire spring coil located on the post...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE CONV FB CR TB TRL SZ3 - 10 INTENDED Recalled by DePuy Orthopaedics,...
The Issue: Potential for the Balseal, a small wire spring coil located on the post...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE CONV RP PS TB TRL SZ10 INTENDED USE: The Recalled by DePuy...
The Issue: Potential for the Balseal, a small wire spring coil located on the post...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE RP CR ARTICULATION SURFACE SIZE 3-8 INTENDED USE: The Recalled by...
The Issue: Potential for the Balseal, a small wire spring coil located on the post...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OxySure Model 615 disposable replacement cartridges Recalled by Oxysure...
The Issue: Flow rate of the recalled replacement cartridges does not meet the draft FDA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: On-X Prosthetic Heart Valve Product Usage: Indicated for the replacement...
The Issue: Incorrect product label. The type of Sewing Ring was mislabeled as being a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT c8000 System List Number 01G06-98 Product Usage: The Abbott...
The Issue: The ARCHITECT c8000 instrument contains tubing that does not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JustRight 5mm Reload Recalled by Justright Surgical, LLC Due to JustRight...
The Issue: JustRight Surgical is recalling various lots of JustRight 5mm Stapler...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JustRight 5mm Stapler Recalled by Justright Surgical, LLC Due to JustRight...
The Issue: JustRight Surgical is recalling various lots of JustRight 5mm Stapler...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magnus Hybrid OR Table Column (1180.01B2) used in conjunction with Recalled...
The Issue: There is a potential issue that could result to collision between the C-arm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Helical Blade Inserter for Trochanteric Fixation Nail-ADVANCED (TFNA)...
The Issue: The height of one of the three guiding pins of the Helical Blade Inserter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NDI Disposable Marker Spheres for Brainlab IGS (Image Guided Recalled by...
The Issue: Inadequate curing of adhesive, may cause the two halves of the spheres to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Scientific Solutions Americas Analytical X-ray System. Delta...
The Issue: Higher than published scatter around the probe head when testing some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nakoma-SL Anterior Cervical Plating System's Variable Single Barrel Drill...
The Issue: Inadequate interference between the screw and the plate when screw implanted...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Offset Femoral Alignment Guide 4mm x 6¿ Recalled by Omnilife Science Inc....
The Issue: The markings on both versions of the OFFSET FEMORAL ALIGNMENT GUIDES are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.