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. 1,099 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
1,099 in last 12 months

Showing 1121–1140 of 48,330 recalls

Medical DeviceSeptember 30, 2025· Medline Industries, LP

Recalled Item: MEDLINE convenience kits labeled as: 1) GENERAL LAPAROSCOPY Recalled by...

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· Medline Industries, LP

Recalled Item: MEDLINE convenience kits labeled as: 1) HEAD AND NECK 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· Medline Industries, LP

Recalled Item: MEDLINE convenience kits labeled as: 1) ACH PLASTICS BREAST-LF Recalled by...

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· 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· 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· 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· Medline Industries, LP

Recalled Item: MEDLINE convenience kits labeled as: 1) GYN LAPAROSCOPY CDS #34-RF Recalled...

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· Medline Industries, LP

Recalled Item: MEDLINE convenience kits labeled as: 1) MAJOR VAGINAL HARPER PACK-LF...

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· 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
DrugSeptember 29, 2025· Acuity Specialty Products, Inc.

Recalled Item: Wyandotte Recalled by Acuity Specialty Products, Inc. Due to cGMP...

The Issue: cGMP deviations: The recall was initiated because required receipt testing...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 29, 2025· Acuity Specialty Products, Inc.

Recalled Item: AFCO Recalled by Acuity Specialty Products, Inc. Due to cGMP deviations: The...

The Issue: cGMP deviations: The recall was initiated because required receipt testing...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 29, 2025· Acella Pharmaceuticals, LLC

Recalled Item: Doxycycline Hyclate Tablets Recalled by Acella Pharmaceuticals, LLC Due to...

The Issue: Failed dissolution specifications: Stability testing found that the lot did...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 29, 2025· Medline Industries, LP

Recalled Item: Medline Recalled by Medline Industries, LP Due to Subpotent Drug

The Issue: Subpotent Drug

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 26, 2025· Dr. Reddy's Laboratories, Inc.

Recalled Item: Succinylcholine Chloride Injection Recalled by Dr. Reddy's Laboratories,...

The Issue: Out-of-Specification (OOS) result during the 6-month stability testing;...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 26, 2025· GE Healthcare Finland Oy

Recalled Item: B105P Recalled by GE Healthcare Finland Oy Due to Potential loss of...

The Issue: Potential loss of monitoring on affected monitors when powered by certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· GE Healthcare Finland Oy

Recalled Item: BATTERY FLEX-3S2P 10.8V 18650 LI-ION SMBUS used with affected patient...

The Issue: Potential loss of monitoring on affected monitors when powered by certain...

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
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