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. 2,639 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,639 in last 12 months

Showing 3290132920 of 53,621 recalls

Medical DeviceMarch 9, 2017· Centurion Medical Products Corporation

Recalled Item: OPHTHALMIC DRESSING TRAY The Covidien Curity Oval Eye Pads are Recalled by...

The Issue: Centurion Medical Products is recalling Convenience Kits that contain...

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

Class II — Potential Health HazardOngoing
DrugMarch 8, 2017· Mckesson Medical Surgical

Recalled Item: hydrALAZINE HYDROCHLORIDE INJECTION Recalled by Mckesson Medical Surgical...

The Issue: Temperature Abuse: Certain pieces of these lots distributed by McKesson...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 8, 2017· Isomeric Pharmacy Solution, LLC

Recalled Item: Triamcinolone 40 mg/mL 2 mL Single-Dose Vial for Injection Recalled by...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 8, 2017· Pondini, inc.

Recalled Item: Pecorino Balze Volteranne DOP Societa Agricola Fattoria Lischeto srl...

The Issue: Pecorino Balze Volteranne raw sheeps milk cheese tested positive for...

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 8, 2017· Gerber Products Company dba Nestle Infant Nutrition

Recalled Item: Gerber¿ Pasta Pick-Ups Cheese Ravioli Net Wt 6 oz (170g) Recalled by Gerber...

The Issue: Gerber Products Company is recalling Cheese Ravioli Gerber¿ Pasta Pick-Ups¿...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 8, 2017· Ortho-Clinical Diagnostics

Recalled Item: enGen (TM) Laboratory Automation Systems using all TCAutomation(TM) Software...

The Issue: Software anomaly; Thermo-Fisher Scientific initially discovered and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2017· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur BR assay Cat No. 03896216 Recalled by Siemens...

The Issue: Potential for the ADVIA Centaur Syphilis assay to interfere with the BR (CA...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2017· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur BR assay Cat No. 02419937 Recalled by Siemens...

The Issue: Potential for the ADVIA Centaur Syphilis assay to interfere with the BR (CA...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2017· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur BR assay Cat No. 09010686 Recalled by Siemens...

The Issue: Potential for the ADVIA Centaur Syphilis assay to interfere with the BR (CA...

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

Class II — Potential Health HazardOngoing
DrugMarch 7, 2017· A&H Focal Inc.

Recalled Item: ZHANSHENG WEIGE CHAOYUE XILISHI tablets Recalled by A&H Focal Inc. Due to...

The Issue: Marked Without An Approved NDA/ANDA: FDA analysis found these products to...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 7, 2017· A&H Focal Inc.

Recalled Item: Ye Lang Shen capsules Recalled by A&H Focal Inc. Due to Marked Without An...

The Issue: Marked Without An Approved NDA/ANDA: FDA analysis found these products to...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 7, 2017· A&H Focal Inc.

Recalled Item: Zhonghua Niubian tablets Recalled by A&H Focal Inc. Due to Marked Without An...

The Issue: Marked Without An Approved NDA/ANDA: FDA analysis found these products to...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 7, 2017· A&H Focal Inc.

Recalled Item: LANG YI HAO CHAONONGSUOPIAN tablets Recalled by A&H Focal Inc. Due to Marked...

The Issue: Marked Without An Approved NDA/ANDA: FDA analysis found these products to...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 7, 2017· A&H Focal Inc.

Recalled Item: HU HU SHENG WEI capsules Recalled by A&H Focal Inc. Due to Marked Without An...

The Issue: Marked Without An Approved NDA/ANDA: FDA analysis found these products to...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 7, 2017· A&H Focal Inc.

Recalled Item: Indian God Lotion Spray Bottle Recalled by A&H Focal Inc. Due to Marked...

The Issue: Marked Without An Approved NDA/ANDA: FDA analysis found this product to...

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

Class III — Low RiskOngoing
Refund
DrugMarch 7, 2017· A&H Focal Inc.

Recalled Item: GERMANY BLACK GOLD tablets Recalled by A&H Focal Inc. Due to Marked Without...

The Issue: Marked Without An Approved NDA/ANDA: FDA analysis found these products to...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 7, 2017· A&H Focal Inc.

Recalled Item: LIEN CHAN FOR SEVEN DAYS capsules Recalled by A&H Focal Inc. Due to Marked...

The Issue: Marked Without An Approved NDA/ANDA: FDA analysis found these products to...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 7, 2017· A&H Focal Inc.

Recalled Item: Power V8 Viagra tablets Recalled by A&H Focal Inc. Due to Marked Without An...

The Issue: Marked Without An Approved NDA/ANDA: FDA analysis found these products to...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 7, 2017· A&H Focal Inc.

Recalled Item: Black Ant capsules Recalled by A&H Focal Inc. Due to Marked Without An...

The Issue: Marked Without An Approved NDA/ANDA: FDA analysis found these products to...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 7, 2017· A&H Focal Inc.

Recalled Item: Tiger King tablets Recalled by A&H Focal Inc. Due to Marked Without An...

The Issue: Marked Without An Approved NDA/ANDA: FDA analysis found these products to...

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

Class II — Potential Health HazardOngoing
Refund