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. 2,622 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,622 in last 12 months

Showing 3546135480 of 53,621 recalls

FoodAugust 3, 2016· Whole Foods Market

Recalled Item: Grassfields Leyden Cheese Recalled by Whole Foods Market Due to Potential E....

The Issue: Possible contamination with Shiga toxin-producing E. coli (STEC).

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 3, 2016· Whole Foods Market

Recalled Item: Grassfields Gouda Cheese Recalled by Whole Foods Market Due to Potential E....

The Issue: Possible contamination with Shiga toxin-producing E. coli (STEC).

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 3, 2016· Whole Foods Market

Recalled Item: Grassfields Edam Cheese Recalled by Whole Foods Market Due to Potential E....

The Issue: Possible contamination with Shiga toxin-producing E. coli (STEC).

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 3, 2016· Reckitt Benckiser LLC

Recalled Item: Mucinex Sinus-Max Day Night Recalled by Reckitt Benckiser LLC Due to...

The Issue: Labeling: Label Error on Declared Strength; label on outer carton...

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

Class III — Low RiskOngoing
Refund
DrugAugust 3, 2016· Golden State Medical Supply Inc.

Recalled Item: Venlafaxine Hydrochloride Extended-Release Capsules Recalled by Golden State...

The Issue: Failed Dissolution Specifications: Out-of-specification results in retained...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 3, 2016· Zydus Pharmaceuticals USA Inc

Recalled Item: BuPROPion Hydrochloride Extended-Release Tablets Recalled by Zydus...

The Issue: Failed Dissolution Specifications: Product did not meet dissolution...

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

Class III — Low RiskOngoing
Refund
DrugAugust 3, 2016· Golden State Medical Supply Inc.

Recalled Item: Venlafaxine Hydrochloride Extended-Release Capsules Recalled by Golden State...

The Issue: Failed Dissolution Specifications: Out-of-specification results in retained...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 2, 2016· Actavis Inc

Recalled Item: Acetasol HC (hydrocortisone and acetic acid otic solution USP) Recalled by...

The Issue: Failed Impurities/Degradation Specifications: Out of specification (OOS)...

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

Class III — Low RiskOngoing
Refund
DrugAugust 2, 2016· Actavis Inc

Recalled Item: Hydrocortisone and acetic acid otic solution Recalled by Actavis Inc Due to...

The Issue: Failed Impurities/Degradation Specifications: Out of specification (OOS)...

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 2, 2016· Hologic, Inc

Recalled Item: SureSight Obturator Introducer Localization Systems (ILS) for ATEC in MRI....

The Issue: Tip Breakage at the glue joint between the obturator body and tip

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2016· Alere San Diego, Inc.

Recalled Item: LDX Optical Check Cassettes (OCC) Model Number: 10-228 and 14-535 Recalled...

The Issue: Incorrect expiration date on the magnetic strip that does not match the...

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

Class III — Low RiskOngoing
Medical DeviceAugust 2, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo Plaza picture archiving and communication system (PAC) (PACS) intended...

The Issue: Siemens is releasing a Customer Advisory Notice to explain meaning of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2016· Greatbatch Medical

Recalled Item: Greatbatch Recalled by Greatbatch Medical Due to On December 17, 2015,...

The Issue: On December 17, 2015, Greatbatch discovered that the Standard Offset Cup...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 2, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.Plaza VB 10 A Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Siemens is releasing a Customer Advisory Notice to explain meaning of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2016· Randox Laboratories Ltd.

Recalled Item: Randox Lipase (Colorimetric) Product Usage: A lipase test system is Recalled...

The Issue: According to the firm carry over was observed when the Lipase test is run...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2016· Becton Dickinson & Company

Recalled Item: catalog # 405612 BD Spinal Anesthesia Tray 22G x 3.5 Recalled by Becton...

The Issue: A recall was initiated by Hospira, Inc. for several lots of 5% Lidocaine HCI...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2016· Bayer Healthcare

Recalled Item: Certegra Workstation used in conjunction with Medrad Stellant CT Injection...

The Issue: CertegraWorkstation when used in conjunction with the Medrad Stellant CT...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2016· Hologic, Inc

Recalled Item: SureSight Obturator Introducer Localization Systems (ILS) for ATEC in MRI....

The Issue: Tip Breakage at the glue joint between the obturator body and tip

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2016· Ethicon, Inc.

Recalled Item: ETHICON MERSILENE" Tape (also to as MERSILENETM Polyester Fiber Recalled by...

The Issue: ETHICON MERSILENE" Tape (also to as MERSILENETM Polyester Fiber Strip or...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: YSIO Max Product Usage: The Ysio Max is a radiographic Recalled by Siemens...

The Issue: Siemens became aware of a potential issue with the patient table for Ysio...

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

Class II — Potential Health HazardOngoing