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 15811600 of 48,330 recalls

Medical DeviceAugust 13, 2025· Beckman Coulter Inc.

Recalled Item: UniCel DxH 900 COULTER Cellular Analysis System Recalled by Beckman Coulter...

The Issue: Hematology analyzers configured with HGB photometers may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2025· Beckman Coulter Inc.

Recalled Item: UniCel DxH 690T COULTER Cellular Analysis System Recalled by Beckman Coulter...

The Issue: Hematology analyzers configured with HGB photometers may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2025· Beckman Coulter Inc.

Recalled Item: UniCel DxH 600 COULTER Cellular Analysis System Recalled by Beckman Coulter...

The Issue: Hematology analyzers configured with HGB photometers may result in...

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

Class II — Potential Health HazardOngoing
FoodAugust 12, 2025· Wegmans Food Markets, Inc.

Recalled Item: Wegmans Medium Camembert Soft Ripened Cheese - 8.8oz - Round wooded...

The Issue: Products may be contaminated with Listeria monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 12, 2025· Wegmans Food Markets, Inc.

Recalled Item: Wegmans Grilling Camembert with Tapenade & Roasted Tomatoes - 10 Recalled by...

The Issue: Products may be contaminated with Listeria monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 12, 2025· Wegmans Food Markets, Inc.

Recalled Item: Wegmans Assorted Cheese Flight - Varies (sold by the lb) Recalled by Wegmans...

The Issue: Products may be contaminated with Listeria monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 12, 2025· Wegmans Food Markets, Inc.

Recalled Item: Wegmans Caramel Apple Pecan Topped Brie Cheese -Small - 13 Recalled by...

The Issue: Products may be contaminated with Listeria monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 12, 2025· VIONA PHARMACEUTICALS INC

Recalled Item: Tavaborole Topical Solution 5% Recalled by VIONA PHARMACEUTICALS INC Due to...

The Issue: Discoloration

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 12, 2025· Max Mobility LLC

Recalled Item: Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial use Recalled by Max...

The Issue: Due to a faulty electrical connection between the speed control Dial and the...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 12, 2025· Max Mobility LLC

Recalled Item: Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial use Recalled by Max...

The Issue: Due to a faulty electrical connection between the speed control Dial and the...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 12, 2025· Max Mobility LLC

Recalled Item: Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial use Recalled by Max...

The Issue: Due to a faulty electrical connection between the speed control Dial and the...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 12, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Pheno. Image-Intensified Flouroscopic X-Ray System. Recalled by...

The Issue: Limited system movements after startup .

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

Class II — Potential Health HazardOngoing
DrugAugust 11, 2025· Lannett Company Inc.

Recalled Item: Lisdexamfetamine Dimesylate Capsules Recalled by Lannett Company Inc. Due to...

The Issue: Labeling: Label Mix-up. A bottle labeled as Lisdexamphetamine Dimesylate...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 11, 2025· Agilent Technologies Denmark ApS

Recalled Item: Brand Name: FLEX Monoclonal Mouse Anti-Human CD20cy Recalled by Agilent...

The Issue: Their is the potential for weak staining which may result in false negative...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2025· Agilent Technologies Denmark ApS

Recalled Item: Brand Name: FLEX Monoclonal Mouse Anti-Human CD20cy Recalled by Agilent...

The Issue: Their is the potential for weak staining which may result in false negative...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2025· Agilent Technologies Denmark ApS

Recalled Item: Brand Name: FLEX Monoclonal Mouse Anti-Human CD20cy Recalled by Agilent...

The Issue: Their is the potential for weak staining which may result in false negative...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2025· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Urinary/Cerebrospinal Fluid Protein (UCFP). Material Number:...

The Issue: Potential for falsely depressed patient, quality control (QC), and/or...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2025· Merge Healthcare, Inc.

Recalled Item: Merge Hemo Recalled by Merge Healthcare, Inc. Due to Merge Healthcare has...

The Issue: Merge Healthcare has been informed by Schiller AG (Baar, Switzerland) of an...

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

Class II — Potential Health HazardOngoing
DrugAugust 8, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Theophylline extended-release tablets 400mg Recalled by Glenmark...

The Issue: Failed Dissolution Specifications: Failure results (above) were reported for...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 8, 2025· Greiner Bio-One North America, Inc.

Recalled Item: Greiner BIO-ONE VACUETTE 2 ml 9NC Coagulation sodium citrate 3.2% Recalled...

The Issue: Blood collection tubes were manufactured with the label applied too high on...

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

Class II — Potential Health HazardOngoing