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

48,330 total recalls
907 in last 12 months

Showing 42801–42820 of 48,330 recalls

Medical DeviceOctober 11, 2013· Zimmer, Inc.

Recalled Item: 1.5 X 6 CORT SCREW HEX/SE 2.0 X 6 CORT Recalled by Zimmer, Inc. Due to...

The Issue: Zimmer recently conducted a review of all historic packaging validations at...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2013· Zimmer, Inc.

Recalled Item: 2.7 X 6 CORT SCREW/SELFTA 2.7 X 7 CORT SCREW/SELFTA Recalled by Zimmer, Inc....

The Issue: Zimmer recently conducted a review of all historic packaging validations at...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance iCT Computed Tomography X-Ray System Recalled by Philips Medical...

The Issue: If the couch, with the footrest extension attached, is positioned where the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2013· GE Healthcare, LLC

Recalled Item: GE Vivid E9 ultrasound system. GE Vivid E9 is a Recalled by GE Healthcare,...

The Issue: GE became aware of a potential safety issue due to a system slow down and...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2013· GE Healthcare, LLC

Recalled Item: HGE Healthcare Patient Monitor B30 Recalled by GE Healthcare, LLC Due to GE...

The Issue: GE Healthcare has recently become aware of a potential safety issue due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2013· St. Jude Medical

Recalled Item: Safire Duo Ablation Catheter MediGuide Enabled Recalled by St. Jude Medical...

The Issue: St. Jude Medical Cardiovascular and Ablation Technologies Division is...

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

Class II — Potential Health HazardOngoing
FoodOctober 11, 2013· yoders country market

Recalled Item: Custom made gift boxes containing: HONEY ROASTED PEANUTS Recalled by yoders...

The Issue: Honey Roasted Peanuts, packaged in custom gift boxes, contained milk and...

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 11, 2013· Metagenics, Inc.

Recalled Item: Spectrazyme Recalled by Metagenics, Inc. Due to Metagenics is recalling...

The Issue: Metagenics is recalling Spectrazyme because their raw material supplier...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 11, 2013· Sandoz Inc

Recalled Item: Fosinopril Sodium and Hydrochlorothiazide Tablets Recalled by Sandoz Inc Due...

The Issue: Subpotent; Hydrochlorothiazide at the 9 month time point.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 11, 2013· Hospira Inc.

Recalled Item: Propofol Injectable Emulsion Recalled by Hospira Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: Visible particles embedded in the glass...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 11, 2013· Teva Pharmaceuticals USA

Recalled Item: Daunorubicin Hydrochloride Injection Recalled by Teva Pharmaceuticals USA...

The Issue: Presence of Precipitate; precipitation of drug product

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 11, 2013· Hospira Inc.

Recalled Item: 0.5% Bupivacaine HCl and Epinephrine 1:200 Recalled by Hospira Inc. Due to...

The Issue: Lack of assurance of sterility; equipment failure led to potential breach in...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 10, 2013· Pure Edge Nutrition

Recalled Item: Bella Vi AMP'D UP Advanced Weight Loss Dietary Supplement capsules Recalled...

The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 10, 2013· Pure Edge Nutrition

Recalled Item: Bella Vi INSANE Bee Pollen Dietary Supplement Capsules Recalled by Pure Edge...

The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 10, 2013· Pure Edge Nutrition

Recalled Item: Bella Vi BTrim MAX Dietary Supplement capsules Recalled by Pure Edge...

The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 10, 2013· Pure Edge Nutrition

Recalled Item: Bella Vi eXtreme ACCELERATOR Dietary Supplement Capsules Recalled by Pure...

The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 10, 2013· Pure Edge Nutrition

Recalled Item: Bella Vi BTrim ULTIMATE BOOST Dietary Supplement capsules Recalled by Pure...

The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 10, 2013· Pure Edge Nutrition

Recalled Item: Bella Vi INSANE AMP'D Dietary Supplement capsules Recalled by Pure Edge...

The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 10, 2013· Nutrition Center, Inc. dba Nutri-West

Recalled Item: Total Enzyme Recalled by Nutrition Center, Inc. dba Nutri-West Due to...

The Issue: Nutrition Center voluntarily recalled Total Enzymes and Total Probiotics...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 10, 2013· Nutrition Center, Inc. dba Nutri-West

Recalled Item: Total Probiotics Recalled by Nutrition Center, Inc. dba Nutri-West Due to...

The Issue: Nutrition Center voluntarily recalled Total Enzymes and Total Probiotics...

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

Class II — Potential Health HazardOngoing
Refund