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. 2,655 recalls have been distributed to Delaware in the last 12 months.
Showing 7441–7460 of 27,373 recalls
Recalled Item: Stryker INBONE Tibial Tray Recalled by Wright Medical Technology, Inc. Due...
The Issue: The tibial tray lock detail is oversized (larger than specification).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: biokitHSV-2 Rapid Test Recalled by Biokit, S.A. Due to HSV-2 rapid test may...
The Issue: HSV-2 rapid test may report false positive results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K-ASSAY IgA Immunoturbidimetric Assay Recalled by Kamiya Biomedical Company,...
The Issue: IgA Reagent may start showing cloudiness over time, which can affect assay...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo Stitch V-Loc 180 Absorbable Reload Recalled by Covidien, LP Due to...
The Issue: Medtronic has received 210 reports of needles breaking during endoscopic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo Stitch V-Loc PBT Non-Absorbable Reload Recalled by Covidien, LP Due to...
The Issue: Medtronic has received 210 reports of needles breaking during endoscopic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health GEL PACK REUSABLE Recalled by Cardinal Health 200, LLC Due...
The Issue: Users are being informed that the product should not be used on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health INSULATED GEL PACK REUSABLE Recalled by Cardinal Health 200,...
The Issue: Users are being informed that the product should not be used on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health Reusable Gel Pack Recalled by Cardinal Health 200, LLC Due...
The Issue: Users are being informed that the product should not be used on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X-Guide X-Mark Probe Tool -used for registering edentulous patients to...
The Issue: Product missing one of two welds connecting the tip to the shaft, if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health INSULATED GEL PACK REUSABLE Recalled by Cardinal Health 200,...
The Issue: Users are being informed that the product should not be used on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health INSULATED GEL PACK REUSABLE Recalled by Cardinal Health 200,...
The Issue: Users are being informed that the product should not be used on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health GEL PACK REUSABLE Recalled by Cardinal Health 200, LLC Due...
The Issue: Users are being informed that the product should not be used on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health HOT AND COLD GEL PACK REUSABLE Recalled by Cardinal Health...
The Issue: Users are being informed that the product should not be used on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health INSULATED GEL PACK REUSABLE Recalled by Cardinal Health 200,...
The Issue: Users are being informed that the product should not be used on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zio AT Clinical Manual Recalled by iRhythm Technologies, Inc. Due to...
The Issue: Ambulatory ECG monitoring system labeling update: 1) Clinically actionable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPEED 9X10X10mm Continuous Compression Implant Recalled by Synthes (USA)...
The Issue: The subject products are being recalled because they contain the incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Synthes Hammertoe Continuous Compression Implants Recalled by Synthes...
The Issue: The subject products are being recalled because they contain the incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPEEDSHIFT20x20x20 Offset 10mm Implant Drill Kit Recalled by Synthes (USA)...
The Issue: The subject products are being recalled because they contain the incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPEED 15X12X12mm Continuous Compression Implant Recalled by Synthes (USA)...
The Issue: The subject products are being recalled because they contain the incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GaGa Pro Lighting Equipment Co. Ltd. manufactures Class IV Laser Recalled by...
The Issue: GAGA Pro LLS systems was not in compliance with the FDA's Performance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.