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: 11,781 cases (589,050 units) Lot/code info: SKU/UDI-Device Identifier: 2008S/00748426002535; Lot Numbers: 210924,190828,190828,190312,190527,190507,190528,190507,181022,190527,181224,190717,181226,181225,190312,190828,190410,180828,190527,190528,180828,181226,211115,210924,210922,210922,210922,210923,210924,210922,210807,210805,210706,210706,210922,210706,210804,210804,210419,210419,210419,210415,210415,210415,210416,210416,210419,210104,210104,210104,201111,201111,201110,201110,201113,201113,201113,201113,201112,201112,201112,201112,201112,201113,201019,201019,201019,200818,200818,200818,200818,200818,200702,200702,200702,200702,190528,190312,181022,190527,190828,181225,181224,190410,190829,181224,180828,190527,190312,181022,181022,181226,190718,180828,190528,190313,190527,181224,181226,181226,190717,181225,181226,230628,230626,230608,230623,230608,230626,230607,230509,230605,230605,230605,230509,230509,230324,230324,230326,230325,230325,221117,221117,221112,221112,221112,221006,211116,211115,211115,211115,220525,220525,220417,220406,220527,220527,220527,220527,220530,220527,220530,220407,220405,220407,220103,220103,220102,220102,220102,181226,190410,190507,190410,211116,211117,210924,210922,210924,210922,210922,210923,210923,210807,210924,210807,210807,210924,210706,210924,210706,210706,210805,210419,210804,210706,210419,210419,210415,210415,210416,210416,210415,210416,210416,210104,210104,210419,210104,201111,201111,201111,201110,201110,201110,201113,201113,201112,201020,201019,200818,190527,190410,230628,230628,230
00748426002535
Official record: FDA (Device enforcement) ↗
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