CLASS II Device recall · Reported 15 Apr 2020 · FDA Enforcement Report
StageOne, Shoulder Cement Spacer Mold, Silicone, Sterile recalled
Biomet is recalling Biomet StageOne, Shoulder Cement Spacer Mold, Silicone, Sterile, distributed in 49 states. The recall was initiated on 26 Feb 2020 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-1657-2020
- FDA event ID
- 85153
- Recalling firm
- Biomet, Warsaw, IN
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 26 Feb 2020
- FDA classified
- 3 Apr 2020
- Reported
- 15 Apr 2020
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Mold
- Device type
- Other Medical Devices
Timeline
| 26 Feb 2020 | Recall initiated by company | |
| 3 Apr 2020 | Classified by FDA | +37 days |
| 15 Apr 2020 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Potentially insufficient cleaning process or potential inadequate process monitoring for cleaning parameters.
Product as listed by the FDA
BIOMET StageOne, Shoulder Cement Spacer Mold 6 MM, 42 X 18 X 46 MM, Silicone, Sterile, Item 431406.
Where it was distributed
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, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin, West Virginia, Wyoming, and the District of Columbia.
AlaskaAlabamaArkansasArizonaCaliforniaColoradoConnecticutDistrict of ColumbiaDelawareFloridaGeorgiaHawaiiIowaIdahoIllinoisIndianaKansasKentuckyLouisianaMassachusetts
Stores named: Walmart
Questions about this recall
Is StageOne, Shoulder Cement Spacer Mold, Silicone, Sterile recalled?
Yes. Biomet recalled StageOne, Shoulder Cement Spacer Mold, Silicone, Sterile on 26 Feb 2020. The recall is Class II and its status is Terminated. Recall number Z-1657-2020.
Why was it recalled?
Potentially insufficient cleaning process or potential inadequate process monitoring for cleaning parameters.
Which lots are affected?
***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)200331(10)518970, (01)00880304551107(17)200430(10)024030, (01)00880304551107(17)200501(10)030980, (01)00880304551107(17)200515(10)166060, (01)00880304551107(17)200521(10)219540, (01)00880304551107(17)200522(10)219550, (01)00880304551107(17)200522(10)219570, (01)00880304551107(17)200611(10)429550, (01)00880304551107(17)200901(10)296820, (01)00880304551107(17)200901(10)296830, (01)00880304551107(17)200901(10)296840, (01)00880304551107(17)200901(10)296850, (01)00880304551107(17)200902(10)298770, (01)00880304551107(17)201109(10)041360, (01)00880304551107(17)201110(10)041370, (01)00880304551107(17)201109(10)041380, (01)00880304551107(17)201119(10)146580, (01)00880304551107(17)201119(10)146590, (01)00880304551107(17)201218(10)443590, (01)00880304551107(17)210126(10)844530, (01)00880304551107(17)210217(10)115350, (01)00880304551107(17)210227(10)251890, (01)00880304551107(17)210307(10)326910, (01)00880304551107(17)210330(10)630420, (01)00880304551107(17)210419(10)870230, (01)00880304551107(17)210606(10)389150, (01)00880304551107(17)210622(10)572890, (01)00880304551107(17)210701(10)698780, (01)00880304551107(17)210725(10)970100, (01)00880304551107(17)210808(10)199840, (01)00880304551107(17)210908(10)481720, (01)00880304551107(17)220523(10)398100, (01)00880304551107(17)220603(10)398130, (01)00880304551107(17)220603(10)789650, (01)00880304551107(17)220611(10)789640, (01)00880304551107(17)220608(10)877250, (01)00880304551107(17)220630(10)202480, (01)00880304551107(17)220630(10)202490, (01)00880304551107(17)220823(10)398090, (01)00880304551107(17)220825(10)398080, (01)00880304551107(17)220523(10)398100R, (01)00880304551107(17)220603(10)789650R, (01)00880304551107(17)230216(10)256430, (01)00880304551107(17)230221(10)256450, (01)00880304551107(17)230228(10)256440, (01)00880304551107(17)230228(10)323790, (01)00880304551107(17)220823(10)398090R, (01)00880304551107(17)220603(10)398130R, (01)00880304551107(17)210330(10)630420R, (01)00880304551107(17)220611(10)789640R, (01)00880304551107(17)240205(10)349500, (01)00880304551107(17)240228(10)710600, (01)00880304551107(17)240306(10)846440, (01)00880304551107(17)240309(10)846420, (01)00880304551107(17)240309(10)846490, (01)00880304551107(17)240313(10)915380, (01)00880304551107(17)240314(10)915370, (01)00880304551107(17)240317(10)962800, (01)00880304551107(17)240323(10)122840, (01)00880304551107(17)240321(10)995670, (01)00880304551107(17)240321(10)995680, (01)00880304551107(17)240628(10)592030, (01)00880304551107(17)240915(10)467400, (01)00880304551107(17)240914(10)467410, (01)00880304551107(17)240913(10)467420, (01)00880304551107(17)240926(10)736490, (01)00880304551107(17)241009(10)073190, (01)00880304551107(17)241209(10)372270, (01)00880304551107(17)250116(10)107950, (01)00880304551107(17)250123(10)186460, (01)00880304551107(17)250123(10)277550
Where was it sold?
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, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin, West Virginia, Wyoming, and the District of Columbia.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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