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. 1,805 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
1,805 in last 12 months

Showing 2682126840 of 48,330 recalls

Medical DeviceNovember 3, 2017· Alden Optical

Recalled Item: Alden HP49 Toric Daily Wear Soft contact Recalled by Alden Optical Due to...

The Issue: Contact lenses lack sterility assurance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Alden Optical

Recalled Item: Alden HP49 Sphere Daily Wear Soft contact Recalled by Alden Optical Due to...

The Issue: Contact lenses lack sterility assurance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Alden Optical

Recalled Item: Alden Classic 55 Toric Daily Wear Soft contact Recalled by Alden Optical Due...

The Issue: Contact lenses lack sterility assurance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Alden Optical

Recalled Item: Alden HP54 Toric Daily Wear Soft contact Recalled by Alden Optical Due to...

The Issue: Contact lenses lack sterility assurance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Alden Optical

Recalled Item: Alden HP54 Sphere Daily Wear Soft contact Recalled by Alden Optical Due to...

The Issue: Contact lenses lack sterility assurance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Alden Optical

Recalled Item: Alden HP59 Sphere Daily Wear Soft contact Recalled by Alden Optical Due to...

The Issue: Contact lenses lack sterility assurance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Alden Optical

Recalled Item: ASTERA Multifocal Toric Daily Wear Soft contact Recalled by Alden Optical...

The Issue: Contact lenses lack sterility assurance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Beaver-Visitec International Inc.

Recalled Item: bvi Beaver EdgeAhead Safety Knife Recalled by Beaver-Visitec International...

The Issue: The protective shield was retracted, and the blade was exposed.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Beaver-Visitec International Inc.

Recalled Item: bvi Beaver Safety Sideport Knife: (a) 1.0mm Recalled by Beaver-Visitec...

The Issue: The protective shield was retracted, and the blade was exposed.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Beaver-Visitec International Inc.

Recalled Item: bvi Beaver Xstar Safety Crescent Recalled by Beaver-Visitec International...

The Issue: The protective shield was retracted, and the blade was exposed.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Beaver-Visitec International Inc.

Recalled Item: bvi Beaver Optimum Safety Sideport Knife: (a) Straight 15o Recalled by...

The Issue: The protective shield was retracted, and the blade was exposed.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Beaver-Visitec International Inc.

Recalled Item: bvi Beaver Xstar Safety Slit Knife: (a) Recalled by Beaver-Visitec...

The Issue: The protective shield was retracted, and the blade was exposed.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Medtronic Inc.

Recalled Item: Everflex Self-Expanding Peripheral Stent with Entrust Delivery System...

The Issue: Stent length on the label may not match the length of the stent itself.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Volcano Corporation

Recalled Item: Volcano Imaging System s5i Recalled by Volcano Corporation Due to On certain...

The Issue: On certain Impacted Systems, an unexpected Microsoft Windows Security dialog...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2017· Pro-Med Instruments Gmbh

Recalled Item: pmi Recalled by Pro-Med Instruments Gmbh Due to The firm received reports of...

The Issue: The firm received reports of two breakages of the pin tips which occurred...

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

Class II — Potential Health HazardOngoing
FoodNovember 1, 2017· Dutch Valley Food Distributors Inc.

Recalled Item: Dark Chocolate Cashew Recalled by Dutch Valley Food Distributors Inc. Due to...

The Issue: Our supplier, GKI, did not have milk declared as an allergen on an item we...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 1, 2017· Dutch Valley Food Distributors Inc.

Recalled Item: Dark Chocolate Almond Recalled by Dutch Valley Food Distributors Inc. Due to...

The Issue: Our supplier, GKI, did not have milk declared as an allergen on an item we...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 1, 2017· Aurora Products, Inc.

Recalled Item: Dark Chocolate Almonds packaged in: 4 oz. Plastic Pouch Recalled by Aurora...

The Issue: Product contains undeclared milk

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 1, 2017· Aurora Products, Inc.

Recalled Item: Dark Chocolate Turbinado Almonds w/ Sea Salt packaged in : Recalled by...

The Issue: Product contains undeclared milk

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 1, 2017· Aurora Products, Inc.

Recalled Item: Dark Chocolate Coffee beans packaged in Bulk 4 oz. Plastic Recalled by...

The Issue: Product contains undeclared milk

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

Class II — Potential Health HazardOngoing
Refund