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 46881–46900 of 48,330 recalls

Medical DeviceJuly 26, 2012· Philips Medical Systems North America Co. Phillips

Recalled Item: Philips and Laerdal brands of HeartStart HS1 Defibrillator Family Model...

The Issue: Philips determined that it is important to clarify information in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Serial interface module RS-485 Product Usage: The System 1 provides Recalled...

The Issue: Terumo Cardiovascular Systems has received reports of malfunctions involving...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2012· St. Jude Medical

Recalled Item: Eon - 3701 (Wall Charger) and 3711 (Portable Charger). Product Recalled by...

The Issue: St. Jude Medical has informed your doctor that a number of cases have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Interface module for CDl System 500 Product Usage: The Interface Recalled by...

The Issue: Terumo Cardiovascular Systems has received reports of malfunctions involving...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: System 1 base 100/120V The Terumo Advanced Perfusion System 1 Recalled by...

The Issue: Terumo Cardiovascular Systems sent a Safety Advisory (AA-2010-007-C) on...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Serial interface module RS-232 Product Usage: The System 1 provides Recalled...

The Issue: Terumo Cardiovascular Systems has received reports of malfunctions involving...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: System 1 base 220/240V The Terumo Advanced Perfusion System 1 Recalled by...

The Issue: Terumo Cardiovascular Systems sent a Safety Advisory (AA-2010-007-C) on...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2012· Aesculap Implant Systems LLC

Recalled Item: Aesculap S4 Element 4.5mm Polyaxial Screws (ST240T Recalled by Aesculap...

The Issue: There is a possibility that the screw channel that holds the rod in place...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2012· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur Multi-Diluent 1 - Used for automated dilutions...

The Issue: Decrease in onboard dilution recovery when using Multi-Diluent 1 that has...

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

Class II — Potential Health HazardOngoing
FoodJuly 25, 2012· Icrest International LLC

Recalled Item: OYSTER MEAT IQF TINY 40/8OZ PRODUCT OF KOREA Recalled by Icrest...

The Issue: The product has been prepared, packed, or held under insanitary conditions...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 25, 2012· Icrest International LLC

Recalled Item: OYSTER MEAT IQF 6/5# LBS KR PRODUCT OF KOREA Recalled by Icrest...

The Issue: The product has been prepared, packed, or held under insanitary conditions...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 25, 2012· Icrest International LLC

Recalled Item: Brand name is Yatta. OYSTERS 1/2 SHELL 144CT Recalled by Icrest...

The Issue: The product has been prepared, packed, or held under insanitary conditions...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 25, 2012· Icrest International LLC

Recalled Item: OYSTER MEAT IQF LARGE 5/4 LBS PRODUCT OF KOREA Recalled by Icrest...

The Issue: The product has been prepared, packed, or held under insanitary conditions...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 25, 2012· Lloyd Inc. of Iowa

Recalled Item: Levothroid (levothyroxine sodium tablets Recalled by Lloyd Inc. of Iowa Due...

The Issue: Subpotent; 9-month stability interval

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 25, 2012· Lloyd Inc. of Iowa

Recalled Item: Thyro-Tab 0.050 mg. Recalled by Lloyd Inc. of Iowa Due to Subpotent; 9-month...

The Issue: Subpotent; 9-month stability interval

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 25, 2012· American Health Packaging

Recalled Item: Topiramate Tablets Recalled by American Health Packaging Due to Labeling:...

The Issue: Labeling: Label Mix-Up: A typographical error in the product form on the...

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

Class III — Low RiskOngoing
Refund
DrugJuly 25, 2012· Lloyd Inc. of Iowa

Recalled Item: Thyro-Tab 0.075 mg. Recalled by Lloyd Inc. of Iowa Due to Subpotent; 9-month...

The Issue: Subpotent; 9-month stability interval

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 25, 2012· Lloyd Inc. of Iowa

Recalled Item: Levothroid (levothyroxine sodium tablets Recalled by Lloyd Inc. of Iowa Due...

The Issue: Subpotent; 9-month stability interval

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 24, 2012· Cadence Pharmaceuticals

Recalled Item: OFIRMEV (acetaminophen) injection Recalled by Cadence Pharmaceuticals Due to...

The Issue: Presence of Particulate Matter: The firm initiated the recall due to visible...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 24, 2012· Capintec Inc

Recalled Item: Capintec Captus 3000 Thyroid Uptake System Nuclear uptake probe intended...

The Issue: Customers who received a Capintec Captus 3000 Thyroid Uptake System with...

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

Class II — Potential Health HazardOngoing