CPSCJune 9, 2016consumer
AR500 Armor Recalls Level III Body Armor Due to Risk of Gunshot Injury or Death
Official recall recorded by the U.S. Consumer Product Safety Commission.
The hazard
The body armor can fail to meet performance requirements for Level III body armor, allowing a bullet to penetrate, and pose a risk of gunshot injury or death.
What to do
Consumers should immediately stop using the recalled body armor and contact the firm for instructions to receive replacement body armor. AR500 will contact all known purchasers about the recall.
Brands named
ar500 armorlevellevel iiiar500
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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- CPSCChronicle Recalls Power Armor Collectible Helmets Due to Risk of Mold Exposure (Recall Alert)2019-09-19
- FDAFenofibrate Tablets, USP 145 mg, 90-count bottles, Rx only, Manufactured for: Camber Pharmaceuticals, Inc. Piscataway, NJ, 08854, NDC 31722-596-902018-09-12
- FDAIndomethacin Capsules, USP, 50 mg, 100-count bottles, Rx only, Manufactured for: Camber Pharmaceuticals, Inc., Piscataway, NJ 08854; By: Hetero, Hetero Labs Limited, Jeedimetla, Hyderabad - 500 055, India; NDC 31722-543-01.2018-07-18
- FDAAripiprazole Tablets, USP, 10 mg, 30-count bottles, Rx Only, Manufactured for Camber Pharmaceuticals, Inc. Piscataway, NJ 08854, By; Hetero Hetero Labs Limited Unit V Polepallly Jadcheria Mahaboob Nagar - 509 301 India, NDC 31722-827-302018-01-10
- FDASimvastatin Tablets, USP, 40 mg, 1000-count bottle, Rx only, Manufactured for: Camber Pharmaceuticals, Inc., Piscataway, NJ 08854, Manufactured by: Hetero (trademark), Hetero Labs Limited, Jeedimetla, Hyderabad - 500 055, India, NDC 31722-513-102017-12-22
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