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 801820 of 27,373 recalls

Medical DeviceSeptember 30, 2025· Medline Industries, LP

Recalled Item: MEDLINE convenience kits labeled as: 1) BASIC NEURO PACK Recalled by Medline...

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 II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2025· Elekta, Inc.

Recalled Item: Brand Name: Leksell Stereotactic System Product Name: Leksell Vantage...

The Issue: Due to increased risk that paint flakes from the engravings may separate...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2025· IMPRIS Imaging Inc

Recalled Item: IMRIS Operating Suite Recalled by IMPRIS Imaging Inc Due to There is a...

The Issue: There is a potential safety issue associated with the magnet venting paths...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 30, 2025· IMPRIS Imaging Inc

Recalled Item: IMRIS Operating Suite Recalled by IMPRIS Imaging Inc Due to There is a...

The Issue: There is a potential safety issue associated with the magnet venting paths...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 30, 2025· CareFusion 303, Inc.

Recalled Item: BD Pyxis Pro MedStation Main Recalled by CareFusion 303, Inc. Due to...

The Issue: Potential fluid ingress of anesthesia station or med station may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2025· CareFusion 303, Inc.

Recalled Item: Various models of BD Pyxis MedFlex Recalled by CareFusion 303, Inc. Due to...

The Issue: Potential fluid ingress of anesthesia station or med station may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2025· CareFusion 303, Inc.

Recalled Item: Various models of BD Pyxis Pro 7-Drawer Auxiliary Recalled by CareFusion...

The Issue: Potential fluid ingress of anesthesia station or med station may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2025· IMPRIS Imaging Inc

Recalled Item: IMRIS Operating Suite Recalled by IMPRIS Imaging Inc Due to There is a...

The Issue: There is a potential safety issue associated with the magnet venting paths...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 30, 2025· IMPRIS Imaging Inc

Recalled Item: IMRIS Operating Suite Recalled by IMPRIS Imaging Inc Due to There is a...

The Issue: There is a potential safety issue associated with the magnet venting paths...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 30, 2025· CareFusion 303, Inc.

Recalled Item: All Serial Numbers/BD Pyxis CII Safe ES Tower Main Recalled by CareFusion...

The Issue: Potential fluid ingress of anesthesia station or med station may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2025· CareFusion 303, Inc.

Recalled Item: Various models of BD Pyxis Medbank: numbers: 1137-00 1145-00 Recalled by...

The Issue: Potential fluid ingress of anesthesia station or med station may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2025· B BRAUN MEDICAL INC

Recalled Item: Brand Name: Hemodialysis Bloodlines Product Name: STREAMLINE BLOODLINE SET...

The Issue: The potential for micro-air bubbles observed in the bloodline and...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 26, 2025· ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Recalled Item: SAFE-T-FILL End Caps for SAFE-T-FILL Blood Gas Capillaries Recalled by ASP...

The Issue: Due to products manufactured under an inadequate quality system to include...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Recalled Item: SAFE-T-FILL Micro Capillary Blood Collection Recalled by ASP Global, LLC....

The Issue: Due to products manufactured under an inadequate quality system to include...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Recalled Item: SAFE-T-FILL Micro Capillary Blood Collection Recalled by ASP Global, LLC....

The Issue: Due to products manufactured under an inadequate quality system to include...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Recalled Item: SAFE-T-FILL MicroHematocrit Capillary Tubes Recalled by ASP Global, LLC. dba...

The Issue: Due to products manufactured under an inadequate quality system to include...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Recalled Item: SAFE-T-FILL Micro Capillary Blood Collection Recalled by ASP Global, LLC....

The Issue: Due to products manufactured under an inadequate quality system to include...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Recalled Item: SAFE-T-FILL Plastic Blood Gas Capillary Tubes Recalled by ASP Global, LLC....

The Issue: Due to products manufactured under an inadequate quality system to include...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Recalled Item: SAFE-T-FILL Plastic Blood Gas Capillary Tubes Recalled by ASP Global, LLC....

The Issue: Due to products manufactured under an inadequate quality system to include...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Recalled Item: SAFE-T-FILL Micro Capillary Blood Collection Recalled by ASP Global, LLC....

The Issue: Due to products manufactured under an inadequate quality system to include...

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

Class II — Potential Health HazardOngoing