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. 2,642 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,642 in last 12 months

Showing 3048130500 of 53,621 recalls

Medical DeviceJuly 28, 2017· NXTHERA

Recalled Item: Rezum System Recalled by NXTHERA Due to Needle Bond may not be able to...

The Issue: Needle Bond may not be able to withstand the tension force applied when the...

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

Class II — Potential Health HazardOngoing
DrugJuly 28, 2017· PD-Rx Pharmaceuticals, Inc.

Recalled Item: Famotidine USP 20 mg Recalled by PD-Rx Pharmaceuticals, Inc. Due to Failed...

The Issue: Failed Tablet/Capsule Specification: out of specification for tablet weight.

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 28, 2017· SIlver HIlls Bakery

Recalled Item: Aldi liveGfree Gluten Free Classic Soft White Hamburger Buns Recalled by...

The Issue: Undeclared eggs

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 27, 2017· Medtronic Navigation, Inc.

Recalled Item: VCLAS (Visualase Cooled Laser Ablation System) Part Number: 9735559...

The Issue: The VCLAS 3mm, 10mm, and 15mm tip devices were not appropriately tested for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2017· Optovue, Inc.

Recalled Item: iFusion Recalled by Optovue, Inc. Due to FDA determined that a 510(k) is...

The Issue: FDA determined that a 510(k) is needed for the Vault Mapping software (also...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2017· Zimmer Surgical Inc

Recalled Item: A.T.S. 2200TS Tourniquet Systems Recalled by Zimmer Surgical Inc Due to...

The Issue: Updated on-device label and 3 pages of an updated Operator/Service Manual....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2017· Zimmer Surgical Inc

Recalled Item: A.T.S. 4000TS Tourniquet Systems Recalled by Zimmer Surgical Inc Due to...

The Issue: Updated on-device label and 3 pages of an updated Operator/Service Manual....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2017· Optovue, Inc.

Recalled Item: iVue with Normative Database Recalled by Optovue, Inc. Due to FDA determined...

The Issue: FDA determined that a 510(k) is needed for the Vault Mapping software (also...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2017· Optovue, Inc.

Recalled Item: iVue 500 with iScan Recalled by Optovue, Inc. Due to FDA determined that a...

The Issue: FDA determined that a 510(k) is needed for the Vault Mapping software (also...

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

Class II — Potential Health HazardOngoing
FoodJuly 26, 2017· NatureAll-STF Holding, LLC

Recalled Item: Leci-thin-Plus Recalled by NatureAll-STF Holding, LLC Due to Undeclared...

The Issue: Undeclared allergens: soy (lecithin)

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 26, 2017· NatureAll-STF Holding, LLC

Recalled Item: Prostate-Plus Recalled by NatureAll-STF Holding, LLC Due to Undeclared Allergens

The Issue: Undeclared allergens: soy (lecithin)

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 26, 2017· NatureAll-STF Holding, LLC

Recalled Item: Metabo-Plus Recalled by NatureAll-STF Holding, LLC Due to Undeclared Allergens

The Issue: Undeclared allergens: milk (Whey)

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 26, 2017· NatureAll-STF Holding, LLC

Recalled Item: Liver-Plus Recalled by NatureAll-STF Holding, LLC Due to Undeclared Allergens

The Issue: Undeclared allergens: soy (lecithin)

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 26, 2017· NatureAll-STF Holding, LLC

Recalled Item: Thymus Plus Recalled by NatureAll-STF Holding, LLC Due to Undeclared Allergens

The Issue: Undeclared allergens: milk (Colostrum)

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 26, 2017· NatureAll-STF Holding, LLC

Recalled Item: Pancreas-Plus Recalled by NatureAll-STF Holding, LLC Due to Undeclared Allergens

The Issue: Undeclared allergens: soy (lecithin)

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 26, 2017· NatureAll-STF Holding, LLC

Recalled Item: Heart-Plus Recalled by NatureAll-STF Holding, LLC Due to Undeclared Allergens

The Issue: Undeclared allergens: soy (lecithin)

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 26, 2017· NatureAll-STF Holding, LLC

Recalled Item: Acidophilus-Plus Recalled by NatureAll-STF Holding, LLC Due to Undeclared...

The Issue: Undeclared allergens: milk (Colostrum, Dried Yogurt, Whey).

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 26, 2017· Synthes (USA) Products LLC

Recalled Item: 2.5 mm Guide Rod Recalled by Synthes (USA) Products LLC Due to Possible lack...

The Issue: Possible lack of product sterility due to potential gaps/channeling in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2017· Synthes (USA) Products LLC

Recalled Item: 2.5 mm Reaming Rod Recalled by Synthes (USA) Products LLC Due to Possible...

The Issue: Possible lack of product sterility due to potential gaps/channeling in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2017· DePuy Orthopaedics, Inc.

Recalled Item: Concorde Lift Torque Limiting Handle. Must be used with supplemental...

The Issue: Potential for Intra-operative breakage of driver tips

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

Class II — Potential Health HazardOngoing