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 4670146720 of 48,330 recalls

Medical DeviceAugust 23, 2012· Biomet, Inc.

Recalled Item: Optilock T15 AO Driver (3.5mm). Intended Use: The OptiLock Upper Recalled by...

The Issue: Field complaints indicate that recent shipments of the 14-400795 and 36505...

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

Class II — Potential Health HazardOngoing
DrugAugust 23, 2012· Evol Nutrition

Recalled Item: Mojo Nights Recalled by Evol Nutrition Due to Marketed Without an Approved...

The Issue: Marketed Without an Approved NDA/ANDA: The products were found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 23, 2012· Evol Nutrition

Recalled Item: Mojo Nights for Her Recalled by Evol Nutrition Due to Marketed Without an...

The Issue: Marketed Without an Approved NDA/ANDA: The products were found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 23, 2012· Ferring Pharmaceuticals Inc

Recalled Item: Novarel¿ (Chorionic Gonadotropin for injection Recalled by Ferring...

The Issue: Labeling; incorrect or missing insert; Warnings portion of the Package...

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

Class III — Low RiskOngoing
Refund
FoodAugust 22, 2012· Spence & Co., Ltd.

Recalled Item: Spence & Co Ltd brand 8oz Smoked Salmon Trim Recalled by Spence & Co., Ltd....

The Issue: Product tested positive for Listeria monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 22, 2012· Spence & Co., Ltd.

Recalled Item: Wellsley Farms 1 LB Nova Salmon Recalled by Spence & Co., Ltd. Due to...

The Issue: Product tested positive for Listeria monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 22, 2012· Viscot Medical LLC

Recalled Item: Dual Tip Marker Recalled by Viscot Medical LLC Due to Dual Tip Marker has...

The Issue: Dual Tip Marker has inconsistent ink flow on the black permanent ink side.

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

Class III — Low RiskOngoing
Medical DeviceAugust 22, 2012· Smith & Nephew Inc

Recalled Item: 12/14 TAPER HIGH OFFSET NECK USE WITH SMITH & NEPHEW Recalled by Smith &...

The Issue: Modular necks were manufactured out of specification by a vendor; the taper...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2012· DePuy Orthopaedics, Inc.

Recalled Item: S-Rom¿ Total Hip System Poly Liner Packaging: The insert is Recalled by...

The Issue: Orthopaedics, Inc. (DePuy) is issuing a voluntary recall of four lots of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2012· SpineFrontier, Inc.

Recalled Item: S-Lift Implant Guides (also known as S-LIF) Compressor Part Number: Recalled...

The Issue: When using the optional S-LIFT (also known as S-LIF) Implant Guides without...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2012· Remel Inc

Recalled Item: Oxoid Antimicrobial Susceptibility Discs Recalled by Remel Inc Due to The...

The Issue: The firm is recalling the product because the cartridges may contain discs...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2012· Ethicon, Inc.

Recalled Item: ETHICON SURGIFLO HEMOSTATIC MATRIX KIT Plus FlexTip with Thrombin...

The Issue: SURGIFLO Hemostatic Matrix Kit & SURGIFLO Hemostatic Matrix Kit with...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 21, 2012· Vycor Medical, Inc.

Recalled Item: Vycor Medical ViewSite Brain Access System 17mm/ 11mm / 5cm Recalled by...

The Issue: Vycor Medical recalled their VBAS (Vycor Viewsite Brain Access System)...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 21, 2012· Ethicon, Inc.

Recalled Item: ETHICON SURGIFLO HEMOSTATIC MATRIX Distributed by ETHICON ETHICON Recalled...

The Issue: SURGIFLO Hemostatic Matrix Kit & SURGIFLO Hemostatic Matrix Kit with...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 21, 2012· Elekta, Inc.

Recalled Item: Oncentra External Beam 4.1. Radiation treatment planning software designed...

The Issue: During the planning process the beam weights can be changed by the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2012· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Mobilett Mira. Mobile X-Ray System. Recalled by Siemens Medical...

The Issue: During regular product monitoring, Siemens has become aware of a potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2012· Remel Inc

Recalled Item: Oxoid Antimicrobial Susceptibility Test Discs Recalled by Remel Inc Due to...

The Issue: The firm is recalling the product due to some cartridges may contain...

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

Class II — Potential Health HazardOngoing
FoodAugust 21, 2012· American Licorice Co

Recalled Item: Red Vines Black Licorice Twists Recalled by American Licorice Co Due to CA...

The Issue: CA Dept. of Public Health collected random samples of Red Vines Black...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 21, 2012· American Licorice Co

Recalled Item: Original Snaps Classic Chewy Candy Recalled by American Licorice Co Due to...

The Issue: CA Dept. of Public Health collected random samples of Red Vines Black...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 21, 2012· American Licorice Co

Recalled Item: RED VINES Mixed Bites Recalled by American Licorice Co Due to CA Dept. of...

The Issue: CA Dept. of Public Health collected random samples of Red Vines Black...

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

Class II — Potential Health HazardOngoing
Refund