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. 2,694 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
2,694 in last 12 months

Showing 26812700 of 48,330 recalls

DrugMarch 31, 2025· Denver Solutions, LLC DBA Leiters Health

Recalled Item: dexmedeTOMIDine HCl PF Recalled by Denver Solutions, LLC DBA Leiters Health...

The Issue: Lack of Assurance of Sterility: Leaking/damaged syringes.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 31, 2025· Denver Solutions, LLC DBA Leiters Health

Recalled Item: Glycopyrrolate Recalled by Denver Solutions, LLC DBA Leiters Health Due to...

The Issue: Lack of Assurance of Sterility: Leaking/damaged syringes.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 31, 2025· Denver Solutions, LLC DBA Leiters Health

Recalled Item: Ketamine HCl 50mg per 5mL (10 mg per mL) Recalled by Denver Solutions, LLC...

The Issue: Lack of Assurance of Sterility: Leaking/damaged syringes.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 31, 2025· Denver Solutions, LLC DBA Leiters Health

Recalled Item: PHENYLephrine HCl in 0.9% Sodium Chloride Recalled by Denver Solutions, LLC...

The Issue: Lack of Assurance of Sterility: Leaking/damaged syringes.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 31, 2025· B. Braun Medical Inc

Recalled Item: 0.9% Sodium chloride Irrigation USP Recalled by B. Braun Medical Inc Due to...

The Issue: Presence of Particulate Matter

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 31, 2025· Ultra Clean Systems, Inc.

Recalled Item: Ultrasonic Cleaning Systems Triton 36 Model Number 6003000804 Triton 72...

The Issue: During routine preventative maintenance checks, it was revealed that carbon...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2025· AVID Medical, Inc.

Recalled Item: Halyard CHRIST SUTURE KIT. General Procedure Tray Convenience Kit Recalled...

The Issue: An issue with a raw material used to coat some surgical needles that may...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2025· AVID Medical, Inc.

Recalled Item: Halyard RAPIDES E-PACK. Cardiovascular Procedure Convenience Kit. Recalled...

The Issue: An issue with a raw material used to coat some surgical needles that may...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2025· AVID Medical, Inc.

Recalled Item: Halyard SUTURE PACK CABG. Cardiovascular Procedure Convenience Kit. Recalled...

The Issue: An issue with a raw material used to coat some surgical needles that may...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2025· Belmont Instrument LLC

Recalled Item: 3.0 Liter Disposable Set (4 sets/case). Model Number: 903-00032. The...

The Issue: Potential crack in the female connector located on the Heat...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2025· Belmont Instrument LLC

Recalled Item: Hyperthermia Pump Procedure Kit. Model Number: 902-00045. Sterile Recalled...

The Issue: Potential crack in the female connector located on the Heat Exchanger in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2025· Siemens Healthcare Diagnostics Inc

Recalled Item: Stratus CS Acute Care cTNI TestPak.IVD test for cardiac troponin Recalled by...

The Issue: Siemens Healthcare Diagnostics Inc., is recalling their Stratus CS Acute...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2025· Belmont Instrument LLC

Recalled Item: Straight Inflow/Outflow Patient Line Kit. Model Number: 902-00037. Sterile...

The Issue: Potential crack in the female connector located on the Heat Exchanger in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2025· Belmont Instrument LLC

Recalled Item: Straight Inflow/Bifurcated Outflow Line Kit. Model Number: 902-00038....

The Issue: Potential crack in the female connector located on the Heat Exchanger in the...

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

Class II — Potential Health HazardOngoing
FoodMarch 29, 2025· Reser's Fine Foods, Inc.

Recalled Item: Trader Joe's Hot Honey Mustard Dressing (SKU #80152) Recalled by Reser's...

The Issue: Undeclared peanuts, soy, sesame, and wheat.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMarch 28, 2025· Micro-X Ltd.

Recalled Item: Brand Name: Rover Product Name: Mobile X-ray System Model/Catalog Number:...

The Issue: Potential for early life x-ray tube failure for mobile x-ray system due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2025· Micro-X Ltd.

Recalled Item: Brand Name: Rover Product Name: Mobile X-ray System Model/Catalog Number:...

The Issue: Potential for early life x-ray tube failure for mobile x-ray system due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2025· Stryker GmbH

Recalled Item: Guide Wire with Ruler Tube 3x800 mm DIA Recalled by Stryker GmbH Due to The...

The Issue: The metal ring at the end of the Guide Wire with Ruler Tube may detach from...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2025· Stryker GmbH

Recalled Item: Guide Wire with Ruler Tube 3x1000 mm DIA Recalled by Stryker GmbH Due to The...

The Issue: The metal ring at the end of the Guide Wire with Ruler Tube may detach from...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2025· Galt Medical Corporation

Recalled Item: GALT Guidewire Guidewires are intended for use in Recalled by Galt Medical...

The Issue: Due to a potential open seal in the sterile barrier packaging.

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

Class II — Potential Health HazardOngoing