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. 2,603 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,603 in last 12 months

Showing 3934139360 of 53,621 recalls

FoodOctober 5, 2015· Fresca Foods, Incorporated

Recalled Item: Snack Out Loud Sea Salt Crunchy Bean Snacks 1.2 OZ Single Serve Units....

The Issue: Fresca Foods conducted a recall on Snack Out Loud Sea Salt flavored Crunchy...

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 5, 2015· General Mills, Inc

Recalled Item: General Mills Honey Nut Cheerios Recalled by General Mills, Inc Due to...

The Issue: General Mills is recalling several days of production of Cheerios and Honey...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 5, 2015· General Mills, Inc

Recalled Item: General Mills Cheerios Recalled by General Mills, Inc Due to Undeclared Wheat

The Issue: General Mills is recalling several days of production of Cheerios and Honey...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 3, 2015· Skinny Latina LLC

Recalled Item: Skinny Latina Million Dollar Marinade Recalled by Skinny Latina LLC Due to...

The Issue: Undeclared soy

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 2, 2015· General Mills, Inc

Recalled Item: Cascadian Farm Organic Cut Green Beans Recalled by General Mills, Inc Due to...

The Issue: General Mills is recalling a limited quantity of frozen Cascadian Farm Cut...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 2, 2015· C.R. Bard, Inc.

Recalled Item: Antibacterial Hydro Personal Catheter Recalled by C.R. Bard, Inc. Due to...

The Issue: Incorrect unit labeling. The case label and shelf box are correct, Product...

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

Class III — Low RiskOngoing
Medical DeviceOctober 2, 2015· Welch Allyn Inc

Recalled Item: Welch Allyn KleenSpec Corded Illumination System Recalled by Welch Allyn Inc...

The Issue: The firm became aware that the KleenSpec¿ 788 Corded Illuminator has the...

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

Class II — Potential Health HazardOngoing
DrugOctober 1, 2015· MSNV, Inc dba National Video Supply

Recalled Item: Rhino 7 3000 Recalled by MSNV, Inc dba National Video Supply Due to...

The Issue: Marketed without an Approved NDA/ANDA: Products contain undeclared active...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 1, 2015· MSNV, Inc dba National Video Supply

Recalled Item: Rhino 7 Platinum 3000 Recalled by MSNV, Inc dba National Video Supply Due to...

The Issue: Marketed without an Approved NDA/ANDA: Products contain undeclared active...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 1, 2015· Tribute Pharmaceuticals US Inc.

Recalled Item: Fenofibric Acid Tablets 105 mg Recalled by Tribute Pharmaceuticals US Inc....

The Issue: Chemical Contamination: The product may contain trace amounts of...

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

Class III — Low RiskOngoing
Refund
DrugOctober 1, 2015· Tribute Pharmaceuticals US Inc.

Recalled Item: Fenofibric Acid Tablets Recalled by Tribute Pharmaceuticals US Inc. Due to...

The Issue: Chemical Contamination: The product may contain trace amounts of...

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

Class III — Low RiskOngoing
Refund
FoodOctober 1, 2015· Kontos Foods Inc.

Recalled Item: Kontos Falafel Mix Net Wt. 5 LBS. (2.27kg) Distributed by Kontos Foods Inc....

The Issue: Kontos Falafel Mix contains undeclared wheat allergen.

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 1, 2015· Sobisk Foods LLC

Recalled Item: Sobisk Lemon Cream Cookies Recalled by Sobisk Foods LLC Due to Undeclared Color

The Issue: Lemon Cream Cookies imported from India, contain undeclared color - FD & C...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 1, 2015· Sobisk Foods LLC

Recalled Item: Sobisk Orange Cream Cookies Recalled by Sobisk Foods LLC Due to Undeclared...

The Issue: Orange Cream Cookies, imported from India, contain undeclared colors...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 1, 2015· Sobisk Foods LLC

Recalled Item: Sobisk Strawberry Cream Cookies Recalled by Sobisk Foods LLC Due to...

The Issue: Strawberry Cream Cookies, imported from India, contain undeclared colors...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 1, 2015· Merge Healthcare, Inc.

Recalled Item: Merge Cardio software. Merge Cardio is a system intended to Recalled by...

The Issue: Reporting feature times out after inactivity for more than an hour sending...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2015· Philips Electronics North America Corporation

Recalled Item: Philips X-Ray Systems Recalled by Philips Electronics North America...

The Issue: Upon initiating Fluoroscopy the user may encounter a user message Fluoro...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2015· Powers Medical Devices, LLC

Recalled Item: The "Pacifier Activated Lullaby" (PAL) System composed of three major...

The Issue: PAL unit has undergone significant technological changes since the previous...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2015· WalkMed Infusion, LLC

Recalled Item: Triton Infusion Pump (model 300000) and Triton fp Infusion Pump Recalled by...

The Issue: The device might fail to detect air in line while infusing the medication...

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

Class II — Potential Health HazardOngoing
DrugSeptember 30, 2015· Premiere Sales Group

Recalled Item: Rhino 7 3000 Recalled by Premiere Sales Group Due to Undeclared Active

The Issue: Marketed without an Approved NDA/ANDA: Products contain undeclared active...

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

Class I — Serious Health HazardOngoing
Refund