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. 2,403 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
2,403 in last 12 months

Showing 581600 of 48,330 recalls

Medical DeviceDecember 2, 2025· Zimmer, Inc.

Recalled Item: Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus...

The Issue: Affected implants may have undersized distal diameter along length of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2025· Microbiologics Inc

Recalled Item: KWIK-STIK 6-Pack Recalled by Microbiologics Inc Due to Affected units may...

The Issue: Affected units may fail to recover the target microorganism Campylobacter...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2025· Zimmer, Inc.

Recalled Item: Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus...

The Issue: Affected implants may have undersized distal diameter along length of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2025· Zimmer, Inc.

Recalled Item: Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus...

The Issue: Affected implants may have undersized distal diameter along length of the...

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

Class II — Potential Health HazardOngoing
FoodDecember 2, 2025· Fazt & Loud LLC

Recalled Item: Lost and Found Energy Recalled by Fazt & Loud LLC Due to Recall is due to a...

The Issue: Recall is due to a misprint on the label that incorrectly identifies the...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 2, 2025· Zimmer, Inc.

Recalled Item: Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus...

The Issue: Affected implants may have undersized distal diameter along length of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2025· Zimmer, Inc.

Recalled Item: Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus...

The Issue: Affected implants may have undersized distal diameter along length of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2025· HANGZHOU BEVER MEDICAL DEVICES CO., LTD.

Recalled Item: BD Ready-to-Use Hydrophilic Catheter 14 Fr (4.7 mm) Straight Tip Recalled by...

The Issue: Labeling error, Incorrect expiration date

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 28, 2025· Baxter Healthcare Corporation

Recalled Item: SIGMA Spectrum Infusion Pump Recalled by Baxter Healthcare Corporation Due...

The Issue: Certain pumps have potentially been released from service with defective...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2025· Medline Industries, LP

Recalled Item: Medline Kits containing B. Braun IV Administration Sets and Pump Recalled by...

The Issue: Medline kits contain B. Braun IV Administration Sets and Pump Administration...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2025· Medline Industries, LP

Recalled Item: Medline Kits containing B. Braun IV Administration Sets and Pump Recalled by...

The Issue: Medline kits contain B. Braun IV Administration Sets and Pump Administration...

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

Class II — Potential Health HazardOngoing
DrugNovember 26, 2025· Golden State Medical Supply Inc.

Recalled Item: Baclofen Tablets USP Recalled by Golden State Medical Supply Inc. Due to...

The Issue: Presence of Foreign Tablets/Capsules

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 26, 2025· Remote Diagnostic Technologies Ltd.

Recalled Item: Philips Tempus Pro Patient Monitor Recalled by Remote Diagnostic...

The Issue: Patient monitor measures Intracranial Pressure (ICP) and Bladder Pressure...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2025· Medline Industries, LP

Recalled Item: Medline Kits containing B. Braun IV Administration Sets and Pump Recalled by...

The Issue: Medline kits contain B. Braun IV Administration Sets and Pump Administration...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2025· Medline Industries, LP

Recalled Item: Medline Kits containing B. Braun IV Administration Sets and Pump Recalled by...

The Issue: Medline kits contain B. Braun IV Administration Sets and Pump Administration...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2025· Beckman Coulter, Inc.

Recalled Item: Beckman Coulter UniCel Dxl 600 Recalled by Beckman Coulter, Inc. Due to...

The Issue: Beckman Coulter has determined that, due to a potential communication issue,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2025· Beckman Coulter, Inc.

Recalled Item: Beckman Coulter UniCel Dxl 800 Recalled by Beckman Coulter, Inc. Due to...

The Issue: Beckman Coulter has determined that, due to a potential communication issue,...

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

Class II — Potential Health HazardOngoing
DrugNovember 26, 2025· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Clindamycin Phosphate USP Recalled by SUN PHARMACEUTICAL INDUSTRIES INC Due...

The Issue: Failed Impurities/Degradation: Out of Specification results for Total...

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

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 26, 2025· Medline Industries, LP

Recalled Item: Medline Kits containing B. Braun IV Administration Sets and Pump Recalled by...

The Issue: Medline kits contain B. Braun IV Administration Sets and Pump Administration...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2025· Medline Industries, LP

Recalled Item: Medline Kits containing B. Braun IV Administration Sets and Pump Recalled by...

The Issue: Medline kits contain B. Braun IV Administration Sets and Pump Administration...

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

Class II — Potential Health HazardOngoing