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. 960 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
960 in last 12 months

Showing 32381–32400 of 48,330 recalls

FoodJune 3, 2016· Post Consumer Brands

Recalled Item: Post Great Grains Protein Blend Recalled by Post Consumer Brands Due to...

The Issue: Post Great Grains Protein Blend - honey oats & seeds cereal is being...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 3, 2016· Dr. Reddy's Laboratories, Inc.

Recalled Item: Sirolimus Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...

The Issue: Failed impurities/degradation: out of specification result for impurity...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 3, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Orthopaedics Trident Constrained Liner Inserter/Impactor Tip...

The Issue: Impactors do not meet the required sterility assurance level (SAL) of 10-6...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2016· Parker Medical

Recalled Item: Parker Trach-Vac Endotracheal Tubes. Tyvek pouches Recalled by Parker...

The Issue: Parker Medical announces a voluntary field action for the Parker Trach-Vac...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2016· ORTHO-CLINICAL DIAGNOSTICS

Recalled Item: VITROS Immunodiagnostic Products Total T4 Reagent Pack Recalled by...

The Issue: Ortho-Clinical Diagnostics confirmed that sample results generated from...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2016· Arrow International Inc

Recalled Item: ARROW Recalled by Arrow International Inc Due to Arrow is recalling these...

The Issue: Arrow is recalling these products due to the possibility that although the...

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

Class II — Potential Health HazardOngoing
FoodJune 2, 2016· The Quaker Oats Company

Recalled Item: Quaker Quinoa Granola Bars Recalled by The Quaker Oats Company Due to...

The Issue: SunOpta expanded their recall of listeria Monocytogenes in sunflower...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 2, 2016· The Quaker Oats Company

Recalled Item: Quaker quinoa granola bars Recalled by The Quaker Oats Company Due to...

The Issue: SunOpta expanded their recall of listeria Monocytogenes in sunflower...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 2, 2016· Ach Food Companies Inc

Recalled Item: Salad topping labeled under the following brand names: (Product 1) Recalled...

The Issue: Product manufactured with ingredient which may be contaminated with Listeria...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 2, 2016· Exact-Rx Inc

Recalled Item: Urea (50% Urea in a Cream Base) Recalled by Exact-Rx Inc Due to...

The Issue: Crystallization; complaints received by the manufacturer of crystals forming...

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

Class III — Low RiskOngoing
Refund
DrugJune 1, 2016· Aidarex Pharmaceuticals LLC

Recalled Item: Ciprofloxacin OPTH 0.3% SOL Recalled by Aidarex Pharmaceuticals LLC Due to...

The Issue: Failed Impurities/Degradation Specifications: Out of specification results...

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

Class III — Low RiskOngoing
Refund
DrugMay 31, 2016· Teva North America

Recalled Item: mitoXANTRONE Injection USP (concentrate) Recalled by Teva North America Due...

The Issue: Failed Impurities/Degradation Specifications: High out of specification...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 31, 2016· Pentax of America Inc

Recalled Item: Pentax Video Bronchoscope Designed to be used with a Pentax Recalled by...

The Issue: Pentax America Inc. is recalling various bronchoscopes which contain an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2016· Pentax of America Inc

Recalled Item: Ultrasound Video Bronchoscope The EB-1970UK Recalled by Pentax of America...

The Issue: The EB-1970UK Ultrasound Video Bronchoscope shipped between the clearance...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2016· Draeger Medical, Inc.

Recalled Item: Oxylog 3000 Recalled by Draeger Medical, Inc. Due to Isolated episodes of...

The Issue: Isolated episodes of leakage at the check valve were found

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 31, 2016· Hologic, Inc

Recalled Item: ATEC CANISTER. Suction Canister with Lid 490 cc. Recalled by Hologic, Inc...

The Issue: Cracks ATEC Canister Lids.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2016· Synthes (USA) Products LLC

Recalled Item: Part # SD313.012 Recalled by Synthes (USA) Products LLC Due to DePuy Synthes...

The Issue: DePuy Synthes is voluntarily initiating this recall due to affected devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2016· Synthes (USA) Products LLC

Recalled Item: Part #313.221 Recalled by Synthes (USA) Products LLC Due to DePuy Synthes is...

The Issue: DePuy Synthes is voluntarily initiating this recall due to affected devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2016· Synthes (USA) Products LLC

Recalled Item: Part # 313.232 Recalled by Synthes (USA) Products LLC Due to DePuy Synthes...

The Issue: DePuy Synthes is voluntarily initiating this recall due to affected devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2016· Synthes (USA) Products LLC

Recalled Item: Part # SD313.011 Recalled by Synthes (USA) Products LLC Due to DePuy Synthes...

The Issue: DePuy Synthes is voluntarily initiating this recall due to affected devices...

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

Class II — Potential Health HazardOngoing