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 20812100 of 48,330 recalls

Medical DeviceJune 18, 2025· Stryker Corporation

Recalled Item: Stryker Recalled by Stryker Corporation Due to Due to complaints their is...

The Issue: Due to complaints their is the potential that irrigation solution may leaked...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2025· Medtronic, Inc.

Recalled Item: Medtronic CareLink SmartSync Device Manager Recalled by Medtronic, Inc. Due...

The Issue: In prior SmartSync application versions, the Abort button stopped the test...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2025· Stryker Corporation

Recalled Item: Stryker Recalled by Stryker Corporation Due to Due to complaints their is...

The Issue: Due to complaints their is the potential that irrigation solution may leaked...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2025· Quidel Corporation

Recalled Item: QuickVue: Dipstick Strep A Test: 50T Recalled by Quidel Corporation Due to...

The Issue: Dipstick strep A test has potential for false positive results.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2025· CARIS LIFE SCIENCES

Recalled Item: MI Cancer Seek UDI Code: (01)00860008613325(21)H5HJHDSXF MI Cancer Recalled...

The Issue: Due to an incorrect test results provided that indicated the incorrect drug...

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

Class II — Potential Health HazardOngoing
FoodJune 16, 2025· Mellace Family Brands California Inc

Recalled Item: Wegmans Semi-Sweet Chocolate Nonpareils Recalled by Mellace Family Brands...

The Issue: Undeclared milk

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 16, 2025· Qualgen, LLC

Recalled Item: Testosterone 200 mg Pellet packaged in 1mL amber vials Recalled by Qualgen,...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date: A printing issue...

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

Class III — Low RiskOngoing
Refund
DrugJune 16, 2025· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Lisdexamfetamine Dimesylate Capsules Recalled by SUN PHARMACEUTICAL...

The Issue: Failed Dissolution Specifications: An out of specification results observed...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 16, 2025· B BRAUN MEDICAL INC

Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by B BRAUN MEDICAL INC Due to...

The Issue: Lack of assurance of sterility: pinholes, within the finger boxes used...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 16, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: SwabFlush Prefilled Syringe with ICU Medical SwabCaps Recalled by MEDLINE...

The Issue: SwabFlush syringes are affected by the ICU Medical recall of their SwabCap...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2025· BD SWITZERLAND SARL

Recalled Item: BD PhaSeal Injector Luer (N30C) Recalled by BD SWITZERLAND SARL Due to...

The Issue: Closed system drug transfer devices were shipped to the U.S. market without...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2025· Draeger, Inc.

Recalled Item: SafeStar 90 Plus Filter. Bidirectionally breathing system filter. Recalled...

The Issue: Reports of slow increase of CO2-curve when gas sample is taken from the gas...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 16, 2025· Draeger, Inc.

Recalled Item: SafeStar 55 Plus Filter. Bidirectionally breathing system filter. Recalled...

The Issue: Reports of slow increase of CO2-curve when gas sample is taken from the gas...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 16, 2025· Draeger, Inc.

Recalled Item: SafeStar 60A Plus Filter. Bidirectionally breathing system filter. Recalled...

The Issue: Reports of slow increase of CO2-curve when gas sample is taken from the gas...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 16, 2025· Draeger, Inc.

Recalled Item: HME TwinStar HEPA Plus Filter. Bidirectionally breathing system filter....

The Issue: Reports of slow increase of CO2-curve when gas sample is taken from the gas...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 16, 2025· CooperVision, Inc.

Recalled Item: Biofinity XR Toric Contact Lens Recalled by CooperVision, Inc. Due to Lens...

The Issue: Lens blisters may have an incomplete or leaking seal which may render them...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2025· CooperVision, Inc.

Recalled Item: Biofinity Toric Multifocal Contact Lens Recalled by CooperVision, Inc. Due...

The Issue: Lens blisters may have an incomplete or leaking seal which may render them...

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

Class II — Potential Health HazardOngoing
FoodJune 14, 2025· Wegmans Food Markets, Inc.

Recalled Item: Wegmans brand Mini Muffins Recalled by Wegmans Food Markets, Inc. Due to...

The Issue: Product may contain foreign objects of metal origin.

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 14, 2025· Wegmans Food Markets, Inc.

Recalled Item: Wegmans brand Mini Muffins Recalled by Wegmans Food Markets, Inc. Due to...

The Issue: Product may contain foreign objects of metal origin.

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 14, 2025· Wegmans Food Markets, Inc.

Recalled Item: a. Wegmans brand Mini Muffins Recalled by Wegmans Food Markets, Inc. Due to...

The Issue: Product may contain foreign objects of metal origin.

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

Class II — Potential Health HazardOngoing
Refund