BIOMET StageOne, Shoulder Cement Spacer Mold 6 MM, 42 X 18 X 46 MM, Silicone, Sterile, Item 431406.
Check against the official notice below — it lists the full affected range.
Biomet, Inc. has recalled approximately 230,001 units of the BIOMET StageOne Shoulder Cement Spacer Mold (6 MM, 42 X 18 X 46 MM, Silicone, Sterile) due to a potentially insufficient cleaning process or inadequate process monitoring for cleaning parameters. The affected product was distributed worldwide, including to numerous U.S. states. The recall involves 87 specific lot numbers with corresponding UDI numbers, with expiration dates ranging from 2014 to 2020.
The recall record does not specify a remedy for affected consumers.
Written by software from the official notice below. Not reviewed by a lawyer.
Potentially insufficient cleaning process or potential inadequate process monitoring for cleaning parameters.
Reason for recall: Potentially insufficient cleaning process or potential inadequate process monitoring for cleaning parameters. Distribution: Worldwide distribution. US distribution to the following states: Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nev Quantity: 230,001 Lot/code info: ***Lot Numbers*** 860650, 215420, 555520, 583840, 089450, 283340, 132840, 413160, 058040, 181870, 408950, 409050, 409080, 851260, 234340, 338950, 581670, 201250, 518970, 024030, 030980, 166060, 219540, 219550, 219570, 429550, 296820, 296830, 296840, 296850, 298770, 041360, 041370, 041380, 146580, 146590, 443590, 844530, 115350, 251890, 326910, 630420, 870230, 389150, 572890, 698780, 970100, 199840, 481720, 398100, 398130, 789650, 789640, 877250, 202480, 202490, 398090, 398080, 398100R, 789650R, 256430, 256450, 256440, 323790, 398090R, 398130R, 630420R, 789640R, 349500, 710600, 846440, 846420, 846490, 915380, 915370, 962800, 122840, 995670, 995680, 592030, 467400, 467410, 467420, 736490, 073190, 372270, 107950, 186460, 277550. ***UDI Numbers*** (01)00880304551107(17)141007(10)860650, (01)00880304551107(17)141112(10)215420, (01)00880304551107(17)181231(10)555520, (01)00880304551107(17)181231(10)583840, (01)00880304551107(17)190206(10)089450, (01)00880304551107(17)190221(10)283340, (01)00880304551107(17)190505(10)132840, (01)00880304551107(17)190530(10)413160, (01)00880304551107(17)190725(10)058040, (01)00880304551107(17)190805(10)181870, (01)00880304551107(17)190826(10)408950, (01)00880304551107(17)190826(10)409050, (01)00880304551107(17)190826(10)409080, (01)00880304551107(17)190930(10)851260, (01)00880304551107(17)191104(10)234340, (01)00880304551107(17)191111(10)338950, (01)00880304551107(17)191209(10)581670, (01)00880304551107(17)200318(10)201250, (01)00880304551107(17)2003
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.