During sterile barrier testing performed on the decanter product line, the samples were identified to have pin holes and tears in the packaging film.
Reason for recall: During sterile barrier testing performed on the decanter product line, the samples were identified to have pin holes and tears in the packaging film. Distribution: Distributed nationwide and internationally to Canada, Mexico, New Zealand, Belize, and Hong Kong. Quantity: 10,366 cases (518,300 units) Lot/code info: SKU/UDI-Device Identifier: 2000S/00748426002085; Lot Numbers: 190220,200424,200424,191214,191025,191118,211024,210602,211016,211016,210912,211024,210912,210912,210912,210727,210828,210608,210608,210411,210411,210323,210118,210113,210113,201123,201009,200423,190429,200619,190719,191025,190614,190715,190614,200424,190614,200619,200914,191225,191027,191106,181005,190715,181123,190429,190606,181207,190220,190805,190503,190304,200331,181207,200914,200914,190606,191209,190719,191225,200424,190606,190715,191027,190429,181005,181207,190606,181123,200311,200311,191118,190826,211116,211116,211116,211116,211024,211024,210714,210714,211116,211024,211024,211116,211016,211016,211016,211016,210912,210912,210827,210827,210912,210912,210828,210828,210828,210828,210827,210608,210608,210608,210608,210602,210504,210411,210411,210411,210323,210323,210323,210323,210113,201123,201123,201009,200903,200914,201009,200903,200903,200903,200903,201009,200619,191106,190304,200914,181207,191210,190614,190220,190715,191225,181005,190614,181005,200914,200619,190719,200423,191106,190220,190429,190826,200619,191118,181005,191225,190614,190429,181207,181005,191118,190429,190220,191027,190715,181123,190110,200903,191209,200423,190805,231120,231011,231011,231104,231104,231009,230919,230919,230919,230919,230824,230825,230824,230824,230824,230615,230622,230615,230622,230622,230615,230614,230614,230614,230614,230614,230425,230425,230425,230425,230327,230327,230327,230327,230130,230130,221125,221125,221125,221126,221
00748426002085
Official record: FDA (Device enforcement) ↗
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