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. 2,699 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
2,699 in last 12 months

Showing 281300 of 27,373 recalls

Medical DeviceDecember 16, 2025· Vortex Surgical Inc.

Recalled Item: 25GA Subretinal Injection Cannula VS0220.25 Recalled by Vortex Surgical Inc....

The Issue: There may be voids located in the seal of Tyvek pouches associated with...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2025· Vortex Surgical Inc.

Recalled Item: Oertli 1. 23G Laser Probe OS4 Flex-Tip VK401113 2. 23G Recalled by Vortex...

The Issue: There may be voids located in the seal of Tyvek pouches associated with...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2025· Vortex Surgical Inc.

Recalled Item: Rumex Disposable Diamond Dusted ILM Elevator Recalled by Vortex Surgical...

The Issue: There may be voids located in the seal of Tyvek pouches associated with...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2025· Vortex Surgical Inc.

Recalled Item: Vortex Surgical 25GA Backflush Recalled by Vortex Surgical Inc. Due to There...

The Issue: There may be voids located in the seal of Tyvek pouches associated with...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2025· Vortex Surgical Inc.

Recalled Item: Vortex Surgical TID Pharos Illuminated Depressor Recalled by Vortex Surgical...

The Issue: XXX

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2025· Vortex Surgical Inc.

Recalled Item: Vortex Surgical I2 Injection Kit Recalled by Vortex Surgical Inc. Due to...

The Issue: There may be voids located in the seal of Tyvek pouches associated with...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2025· Medline Industries, LP

Recalled Item: Medline medical procedure convenience kits labeled as: 1) LAVH PROCEDURE...

The Issue: Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2025· Vortex Surgical Inc.

Recalled Item: Vortex Surgical 1. 23GA Laser Probe Curved Cat No. VS0120.23 Recalled by...

The Issue: There may be voids located in the seal of Tyvek pouches associated with...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2025· Medline Industries, LP

Recalled Item: Medline medical procedure convenience kits labeled as: 1) LAPAROSCOPY CDS-LF...

The Issue: Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2025· Medline Industries, LP

Recalled Item: Medline medical procedure convenience kits labeled as: 1) THORACIC ROBOTICS...

The Issue: Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD10F Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...

The Issue: Philips has identified that in a limited number of impacted systems the drip...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2025· Intuitive Surgical, Inc.

Recalled Item: da Vinci SP Recalled by Intuitive Surgical, Inc. Due to Access Port System...

The Issue: Access Port System tray may develop cracks potentially resulting in a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD10/10 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...

The Issue: Philips has identified that in a limited number of impacted systems the drip...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD20 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...

The Issue: Philips has identified that in a limited number of impacted systems the drip...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2025· Hologic, Inc

Recalled Item: Brevera Breast Biopsy System Disposable 9 Gauge Needle. Biopsy Instrument....

The Issue: Presence of particulates in affected devices that can be deposited into...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Product Name: Allura Xper FD10C Recalled by PHILIPS MEDICAL SYSTEMS...

The Issue: Philips has identified that in a limited number of impacted systems the drip...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2025· SunMed Holdings, LLC

Recalled Item: Brand Name: Broselow Product Name: Broselow Pediatric Emergency Rainbow Tape...

The Issue: Product contains potentially harmful dosing errors for Vecuronium,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 15, 2025· Sysmex America, Inc.

Recalled Item: TS-10/TS-10H Tube Sorter Recalled by Sysmex America, Inc. Due to Under...

The Issue: Under specific conditions, the lift's electromagnetic holding force may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2025· SunMed Holdings, LLC

Recalled Item: Brand Name: Broselow Product Name: Broselow Pediatric Emergency Rainbow Tape...

The Issue: Product contains potentially harmful dosing errors for Vecuronium,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 15, 2025· ICU Medical, Inc.

Recalled Item: ICU Medical Plum Duo Infusion Pump Recalled by ICU Medical, Inc. Due to Plum...

The Issue: Plum Solo and Duo Infusion pumps include a feature, that when selected,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing