Product Recalls in New York

Product recalls affecting New York — including food, drugs, consumer products, medical devices, and vehicles distributed to New York. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,842 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,842 in last 12 months

Showing 82418260 of 13,591 recalls

DrugMarch 7, 2017· A&H Focal Inc.

Recalled Item: MAX MAN 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: HARD TEN DAYS 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: GOLD VIGRA 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: Clalis capsules Recalled by A&H Focal Inc. Due to Marked Without An Approved...

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: Miraculous Evil Root 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: DADIYONGSHI XIANGGANGTIANLONGSHENGWU tablets Recalled by A&H Focal Inc. Due...

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: YANSHIJIAONANG 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: 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
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: 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: 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: 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: 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: 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: 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: 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: 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: 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· Alvogen, Inc

Recalled Item: Nifedipine Extended-Release Tablets Recalled by Alvogen, Inc Due to Cross...

The Issue: Cross Contamination with another product:residual powder found in inlet air...

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

Class III — Low RiskOngoing
Refund
DrugMarch 7, 2017· Alvogen, Inc

Recalled Item: Nifedipine Extended-Release Tablets Recalled by Alvogen, Inc Due to Cross...

The Issue: Cross Contamination with another product:residual powder found in inlet air...

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

Class III — Low RiskOngoing
Refund