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. 1,667 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
1,667 in last 12 months

Showing 4672146740 of 48,330 recalls

FoodAugust 21, 2012· Newark Nut Stores, Inc.

Recalled Item: Organic Pine Nuts (Raw Recalled by Newark Nut Stores, Inc. Due to Pine nuts...

The Issue: Pine nuts may contain peanuts

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 21, 2012· J F C International Inc

Recalled Item: Furikake (a Japanese rice seasoning of seaweed flakes with...

The Issue: The firm recalled the product due to undeclared eggs, soybeans, and wheat....

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 21, 2012· Ranbaxy Inc.

Recalled Item: Atorvastatin Calcium Tablets Recalled by Ranbaxy Inc. Due to Adulterated...

The Issue: Adulterated Presence of Foreign Tablets: A product complaint was received by...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 20, 2012· Abbott Vascular

Recalled Item: Armada 35/ Armada 35 LL PTA Catheters. The device is Recalled by Abbott...

The Issue: Abbott Vascular is recalling the Armada 35 and Armada 35 LL PTA Catheters...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 20, 2012· Remel Inc

Recalled Item: Remel Xpect Clostridium difficile Toxin A/B Recalled by Remel Inc Due to The...

The Issue: The firm is recalling the products due to a potential for false negative...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 20, 2012· Microgenics Corporation

Recalled Item: Thermo Scientific MAS Omni IMMUNE and Omni IMMUNE PRO Recalled by...

The Issue: In house testing confirmed that CK-MS and Insulin claimed in both Omni...

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

Class III — Low RiskOngoing
Medical DeviceAugust 20, 2012· Remel Inc

Recalled Item: Remel Xpect Clostridium difficile Toxin A/B Recalled by Remel Inc Due to The...

The Issue: The firm is recalling the products due to a potential for false negative...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 17, 2012· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Orthopaedics Torx 6.5mm Cancellous Bone Screw The Recalled by...

The Issue: Stryker has received reports from the field indicating that certain lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 17, 2012· Vital Signs Colorado Inc.

Recalled Item: Vital Signs Disposable General Purpose 9 French Temperature Probe For...

The Issue: There is a potential for epistaxis during use of the Disposable General...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 17, 2012· Haag-Streit USA Inc

Recalled Item: Octopus 101 Perimeter Recalled by Haag-Streit USA Inc Due to The firm...

The Issue: The firm recalled the device after learning of a possible deviation in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 17, 2012· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Orthopaedics Torx 6.5mm Cancellous Bone Screw The Recalled by...

The Issue: Stryker has received reports from the field indicating that certain lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 17, 2012· Varian Medical Systems, Inc. Oncology Systems

Recalled Item: Varian brand Eclipse Treatment Planning System Recalled by Varian Medical...

The Issue: Varian has identified an anomaly with the Eclipse Treatment Planning where...

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

Class II — Potential Health HazardOngoing
FoodAugust 17, 2012· Protica, Inc

Recalled Item: Protein Shots Recalled by Protica, Inc Due to Product not sufficiently...

The Issue: Product not sufficiently acidified (equilibrium pH higher than 4.6),...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 17, 2012· Protica, Inc

Recalled Item: ProBalance Protein To Go(TM) Recalled by Protica, Inc Due to Product not...

The Issue: Product not sufficiently acidified (equilibrium pH higher than 4.6),...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 17, 2012· Protica, Inc

Recalled Item: Protein Wave 15 grams of protein Recalled by Protica, Inc Due to Product not...

The Issue: Product not sufficiently acidified (equilibrium pH higher than 4.6),...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 17, 2012· Protica, Inc

Recalled Item: ProBalance Protein To Go(TM) Recalled by Protica, Inc Due to Product not...

The Issue: Product not sufficiently acidified (equilibrium pH higher than 4.6),...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 16, 2012· J & J Snack Foods Corporation

Recalled Item: Luigi's Real Italian Ice Birthday Cake 6 FL OZ cups Recalled by J & J Snack...

The Issue: Luigi's Real Italian Ice Birthday Cake Flavor is mislabeled as "Dairy-Free".

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 16, 2012· Karl Storz Endoscopy America Inc

Recalled Item: KARL STORZ Photodynamic Diagnosis (PDD) D-Light C System Recalled by Karl...

The Issue: The recall was initiated because Karl Storz has confirmed that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2012· ZOLL Medical Corporation

Recalled Item: Zoll X Series Defibrillator/Pacemaker/Monitor Product Usage: The product is...

The Issue: Shipped with incorrect software

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2012· Surgical Specialties Puerto Rico Inc. dba Angiotech PR Inc.

Recalled Item: "***Sharpoint IQ Geometry Slit Knife Angled Recalled by Surgical Specialties...

The Issue: Potential for bent tips.

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

Class II — Potential Health HazardOngoing