A&H Focal Inc. recalls

22 recalls on record · latest: February 6, 2018

Official U.S. recall history for A&H Focal Inc., compiled from official government records.

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Dietary Supplements recalled over undeclared pde

February 6, 2018 · Drug & medication recalls Undeclared PDE-5 Inhibitors — Device & Drug Safety

A&H Focal Inc. recalls Zhonghua Niubian tablets, 2000mg, 6-count bottle, labeling is in foreign language

March 7, 2017 · Drug & medication recalls High risk Marked Without An Approved NDA/ANDA: FDA analysis found these products to conta…

A&H Focal Inc. recalls LANG YI HAO CHAONONGSUOPIAN tablets, 500 mg, 8-count bottle, labeling is in foreign language

March 7, 2017 · Drug & medication recalls High risk Marked Without An Approved NDA/ANDA: FDA analysis found these products to conta…

A&H Focal Inc. recalls HU HU SHENG WEI capsules, 3000 mg, 2-count bottle, labeling is in foreign language

March 7, 2017 · Drug & medication recalls High risk Marked Without An Approved NDA/ANDA: FDA analysis found these products to conta…

A&H Focal Inc. recalls Ye Lang Shen capsules, 5000 mg, 8-count bottle, labeling is in foreign language

March 7, 2017 · Drug & medication recalls Moderate risk Marked Without An Approved NDA/ANDA: FDA analysis found these products to conta…

A&H Focal Inc. recalls Indian God Lotion Spray Bottle, labeling is in foreign language

March 7, 2017 · Drug & medication recalls Marked Without An Approved NDA/ANDA: FDA analysis found this product to contain…

A&H Focal Inc. recalls GERMANY BLACK GOLD tablets, 2800 mg, 8-count bottle, labeling is in foreign language

March 7, 2017 · Drug & medication recalls High risk Marked Without An Approved NDA/ANDA: FDA analysis found these products to conta…

A&H Focal Inc. recalls LIEN CHAN FOR SEVEN DAYS capsules, labeling is in foreign language

March 7, 2017 · Drug & medication recalls High risk Marked Without An Approved NDA/ANDA: FDA analysis found these products to conta…

A&H Focal Inc. recalls Black Ant capsules, 4600mg, 4-count blister pack, labeling is in foreign language

March 7, 2017 · Drug & medication recalls Moderate risk Marked Without An Approved NDA/ANDA: FDA analysis found these products to conta…

A&H Focal Inc. recalls Tiger King tablets, labeling is in foreign language

March 7, 2017 · Drug & medication recalls Moderate risk Marked Without An Approved NDA/ANDA: FDA analysis found these products to conta…

A&H Focal Inc. recalls Power V8 Viagra tablets, 200mg, 10-Grain bottle, labeling is in foreign language

March 7, 2017 · Drug & medication recalls High risk Marked Without An Approved NDA/ANDA: FDA analysis found these products to conta…

A&H Focal Inc. recalls YANSHIJIAONANG capsules, 2000mg, 8-count bottle, labeling is in foreign language

March 7, 2017 · Drug & medication recalls High risk Marked Without An Approved NDA/ANDA: FDA analysis found these products to conta…

A&H Focal Inc. recalls DADIYONGSHI XIANGGANGTIANLONGSHENGWU tablets, 6-count bottle, labeling is in foreign language

March 7, 2017 · Drug & medication recalls High risk Marked Without An Approved NDA/ANDA: FDA analysis found these products to conta…

A&H Focal Inc. recalls Miraculous Evil Root capsules, 1200 mg, 6-count bottle, labeling is in foreign language

March 7, 2017 · Drug & medication recalls High risk Marked Without An Approved NDA/ANDA: FDA analysis found these products to conta…

A&H Focal Inc. recalls ZHANSHENG WEIGE CHAOYUE XILISHI tablets, 2000 mg, 6-count bottle, labeling is in foreign language

March 7, 2017 · Drug & medication recalls High risk Marked Without An Approved NDA/ANDA: FDA analysis found these products to conta…

A&H Focal Inc. recalls Clalis capsules, 50mg, 6-count bottle, labeling is in foreign language

March 7, 2017 · Drug & medication recalls High risk Marked Without An Approved NDA/ANDA: FDA analysis found these products to conta…

A&H Focal Inc. recalls GOLD VIGRA capsules, 50mg, 6-count bottle, labeling is in foreign language

March 7, 2017 · Drug & medication recalls High risk Marked Without An Approved NDA/ANDA: FDA analysis found these products to conta…

A&H Focal Inc. recalls HARD TEN DAYS capsules, 4500mg, 6-count bottle, labeling is in foreign language

March 7, 2017 · Drug & medication recalls Moderate risk Marked Without An Approved NDA/ANDA: FDA analysis found these products to conta…

A&H Focal Inc. recalls MAX MAN capsules, 3000 mg, 6-count bottle, labeling is in foreign language

March 7, 2017 · Drug & medication recalls Moderate risk Marked Without An Approved NDA/ANDA: FDA analysis found these products to conta…

A&H Focal Inc. recalls GERMANY NIUBIAN tablets, 3000mg, 10-count bottle, labeling is in foreign language

March 7, 2017 · Drug & medication recalls High risk Marked Without An Approved NDA/ANDA: FDA analysis found these products to conta…

A&H Focal Inc. recalls STREE OVERLORD capsules, 3800 mg, 4-count bottle, labeling is in foreign language

March 7, 2017 · Drug & medication recalls Moderate risk Marked Without An Approved NDA/ANDA: FDA analysis found these products to conta…

A&H Focal Inc. recalls MACA gold tablets, 6800 mg, 10-count bottle, labeling is in foreign language

March 7, 2017 · Drug & medication recalls High risk Marked Without An Approved NDA/ANDA: FDA analysis found these products to conta…