Product Recalls in New Jersey

Product recalls affecting New Jersey — including food, drugs, consumer products, medical devices, and vehicles distributed to New Jersey. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,549 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,549 in last 12 months

Showing 5294152960 of 53,621 recalls

FoodMay 8, 2012· Seoul Shik Poom, Inc.

Recalled Item: Frozen Salted Clam Recalled by Seoul Shik Poom, Inc. Due to Korean Certified...

The Issue: Korean Certified Shippers delisted from ICSSL.

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 8, 2012· Panera Bread LLC

Recalled Item: Panera Recalled by Panera Bread LLC Due to Product ingredient statement...

The Issue: Product ingredient statement reversed for Reduced Fat Honey Walnut Cream...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 8, 2012· Panera Bread LLC

Recalled Item: Panera HONEY WALNUT CREAM CHEESE SPREAD Recalled by Panera Bread LLC Due to...

The Issue: Product ingredient statement reversed for Reduced Fat Honey Walnut Cream...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 8, 2012· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Dimension Vista(R) System B12 Flex(R) Reagent Cartridge (K6442) B12...

The Issue: Siemens Healthcare Diagnostics has confirmed that the presence of Intrinsic...

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

Class II — Potential Health HazardOngoing
DrugMay 7, 2012· Guthy-Renker LLC

Recalled Item: Rodan & Fields Proactiv Solution Recalled by Guthy-Renker LLC Due to...

The Issue: Subpotent Drug: Salicylic acid is subpotent.

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

Class III — Low RiskOngoing
Refund
DrugMay 7, 2012· Guthy-Renker LLC

Recalled Item: Rodan & Fields Proactiv Solution Recalled by Guthy-Renker LLC Due to...

The Issue: Subpotent Drug: Salicylic acid is subpotent.

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

Class III — Low RiskOngoing
Refund
DrugMay 7, 2012· Guthy-Renker LLC

Recalled Item: Rodan & Fields Proactiv Solution Recalled by Guthy-Renker LLC Due to...

The Issue: Subpotent Drug: Salicylic acid is subpotent.

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

Class III — Low RiskOngoing
Refund
DrugMay 7, 2012· Guthy-Renker LLC

Recalled Item: Rodan & Fields Proactiv Solution Recalled by Guthy-Renker LLC Due to...

The Issue: Subpotent Drug: Salicylic acid is subpotent.

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

Class III — Low RiskOngoing
Refund
DrugMay 7, 2012· Guthy-Renker LLC

Recalled Item: Rodan & Fields Proactiv Solution Recalled by Guthy-Renker LLC Due to...

The Issue: Subpotent Drug: Salicylic acid is subpotent.

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

Class III — Low RiskOngoing
Refund
DrugMay 7, 2012· Endo Pharmaceuticals, Inc.

Recalled Item: Endocet (oxycodone and acetaminophen) tablets Recalled by Endo...

The Issue: Adulterated Presence of Foreign Tablets: Customer complaint that some...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 7, 2012· MTI Precision Products LLC.

Recalled Item: Lynx TM20 Torquemaster Low Speed Handpiece MTI Dental Products Recalled by...

The Issue: Sharp edge on the body/housing of the Lynx TM20 TorqueMaster Low Speed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2012· Mindray DS USA, Inc. d.b.a. Mindray North America

Recalled Item: V Series Patient Monitors Recalled by Mindray DS USA, Inc. d.b.a. Mindray...

The Issue: Mindray has identified two software anomalies contained in the V Series...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2012· JK Products & Services, Inc

Recalled Item: BeautyAngel Health Fitness Natural Collagen Stimulation Anti Aging For human...

The Issue: The Beauty Angel was marketed without a 510k.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2012· Civco Medical Instruments Inc

Recalled Item: CIVCO VirtuTRAX Instrument Navigator Recalled by Civco Medical Instruments...

The Issue: The general purpose electromagnetic sensor was incorrectly calibrated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2012· Civco Medical Instruments Inc

Recalled Item: CIVCO General Purpose Sensor Recalled by Civco Medical Instruments Inc Due...

The Issue: The general purpose electromagnetic sensor was incorrectly calibrated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2012· Civco Medical Instruments Inc

Recalled Item: CIVCO General Purpose Sensor Recalled by Civco Medical Instruments Inc Due...

The Issue: The general purpose electromagnetic sensor was incorrectly calibrated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2012· Civco Medical Instruments Inc

Recalled Item: CIVCO General Purpose Sensor Recalled by Civco Medical Instruments Inc Due...

The Issue: The general purpose electromagnetic sensor was incorrectly calibrated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2012· Civco Medical Instruments Inc

Recalled Item: CIVCO VirtuTRAX Instrument Navigator Recalled by Civco Medical Instruments...

The Issue: The general purpose electromagnetic sensor was incorrectly calibrated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2012· Non-Invasive Monitoring Systems, Inc.

Recalled Item: USA-002 Rev A brochure is a two sided tri-fold printed Recalled by...

The Issue: Non-Invasive Monitoring Systems Inc (NIMS) is voluntarily recalling...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2012· Non-Invasive Monitoring Systems, Inc.

Recalled Item: US-001 Rev A brochure is a two sided tri-fold printed Recalled by...

The Issue: Non-Invasive Monitoring Systems Inc (NIMS) is voluntarily recalling...

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

Class II — Potential Health HazardOngoing