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. 2,695 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
2,695 in last 12 months

Showing 12011220 of 27,373 recalls

Medical DeviceJuly 31, 2025· Medline Industries, LP

Recalled Item: Reprocessed Webster CS Catheter 10 Electrodes for electrophysiological...

The Issue: Specific lots of reprocessed electrophysiology and ultrasound catheters may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 31, 2025· Medline Industries, LP

Recalled Item: Reprocessed Inquiry Steerable Diagnostics Catheter for electrogram recording...

The Issue: Specific lots of reprocessed electrophysiology and ultrasound catheters may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 31, 2025· Medline Industries, LP

Recalled Item: Reprocessed ACUSON AcuNav Ultrasound Catheter for intracardiac and...

The Issue: Specific lots of reprocessed electrophysiology and ultrasound catheters may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 31, 2025· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LinkSymphoKnee System Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due...

The Issue: Some modular LinkSymphoKnee TiNbN Tibial Components were manufactured with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2025· Lumicell, Inc.

Recalled Item: Brand Name: 900-00218 Sterile Cover 10-Pack Shipper Box Assembly Product...

The Issue: The potential of the elastic bands included in the kit detaching or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2025· S.I.N. Implant System Ltda

Recalled Item: IMPLANT EPIKUT PLUS MT16 3 Recalled by S.I.N. Implant System Ltda Due to...

The Issue: Dental implants were imported under temperature and storage conditions that...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2025· Contract Medical International GmbH

Recalled Item: Brand Name: Fortress Introducer Sheath System Product Name: Fortress...

The Issue: Units may have been packaged with an incorrect pouch label, which lists the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2025· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Clearview Strep A Exact II Dipstick Respiratory Kit Recalled by Mckesson...

The Issue: Due to a classification error in the inventory management system, specific...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2025· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS Chemistry Products LAC Slides. Catalog Number: 8150112. 1 Sales...

The Issue: VITROS Chemistry Products LAC Slides on VITROS XT 3400 and VITROS XT 7600...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2025· Ortho-Clinical Diagnostics, Inc.

Recalled Item: Chemistry Products LAC Slides. Catalog Number: 8433880. 1 Sales Unit...

The Issue: VITROS Chemistry Products LAC Slides on VITROS XT 3400 and VITROS XT 7600...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2025· ORTOMA AB

Recalled Item: Ortoma Inserter Adapter OTD: Inserter Adapter OTD Straight Recalled by...

The Issue: Due to a weld breakage between the pin and inserter holder of the Inserter...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2025· Zap Surgical Systems

Recalled Item: ZAP-X Radiosurgery System Recalled by Zap Surgical Systems Due to If the...

The Issue: If the radiosurgery system triggers a proximity error message during a long...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline medical convenience kits labeled as: 1. ADULT INTUBATION TRAY...

The Issue: Medline Industries, LP is issuing a recall for specific item(s) and lot(s)...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 25, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline medical convenience kits labeled as: 1. NEWBORN RESUSCITATION KIT...

The Issue: Medline Industries, LP is issuing a recall for specific item(s) and lot(s)...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 25, 2025· Merit Medical Systems, Inc.

Recalled Item: 10Fore Hemostasis Valve Catalog Number / UDI-DI code: MAPTEN4 / Recalled by...

The Issue: Due to a manufacturing issue involving the silicone quad ring where the ring...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2025· Olympus Corporation of the Americas

Recalled Item: Electrosurgical Recalled by Olympus Corporation of the Americas Due to...

The Issue: Potential for the ESG-410 Electrosurgical Generator to display an error...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2025· Olympus Corporation of the Americas

Recalled Item: Electrosurgical Recalled by Olympus Corporation of the Americas Due to...

The Issue: Potential for the ESG-410 Electrosurgical Generator to display an error...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2025· Dexcom, Inc.

Recalled Item: Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name:...

The Issue: The affected devices are the Dexcom G7 Continuous Glucose Monitoring System...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 24, 2025· Dexcom, Inc.

Recalled Item: Brand Name: Dexcom ONE+ Continuous Glucose Monitoring System Product Name:...

The Issue: The affected devices are the Dexcom G7 Continuous Glucose Monitoring System...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 24, 2025· Dexcom, Inc.

Recalled Item: Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name:...

The Issue: The affected devices are the Dexcom G7 Continuous Glucose Monitoring System...

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

Class I — Serious Health HazardOngoing