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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device

Biomet, Inc.: Packaging of various implants may not have sufficient adhesion on all sides, leading to loss of sterile barrier integrity. Use of product poses risk of infection, leading to surgical intervention, and/or extension of surgery to find another part.

Agency Publication Date: March 18, 2022
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Affected Products

Product: BIOMET Sports Medicine JUGGERLOC SLOTTED REAMER: [Item # 110010371, 6MM], [Item #110010372, 7MM], [Item # 110010373, 8MM], [Item #110018275, 5MM]. Devices are packaged in a vacuum sealed nylon pouch, which is placed in a carton with the appropriate IFU and patient record labels. Identifying labels on the pouch and the carton.

29 lots: Lot Number, UDI Number - [061400, (01)00887868465758(17)310630(10)061400], [061410, (01)00887868465758(17)310723(10)061410], [089370, (01)00887868465758(17)310726(10)089370], [260770, (01)00880304857261(17)310917(10)260770], [503410, (01)00880304857285(17)311011(10)503410], [503420, (01)00880304857261(17)310924(10)503420], [503430, (01)00880304857285(17)311011(10)503430], [503450, (01)00880304857261(17)310924(10)503450], [503460, (01)00880304857285(17)311011(10)503460], [503610, (01)00880304857285(17)310924(10)503610], [539370, (01)00880304857285(17)311105(10)539370], [549910, (01)00887868465758(17)310603(10)549910], [577830, (01)00880304857292(17)310917(10)577830], [577840, (01)00880304857292(17)310922(10)577840], [577860, (01)00880304857292(17)310917(10)577860], [637200, (01)00880304857285(17)311027(10)637200], [796600, (01)00880304857285(17)311105(10)796600], [796610, (01)00880304857261(17)311027(10)796610], [886120, (01)00880304857285(17)310805(10)886120], [886200, (01)00880304857285(17)310805(10)886200], [886210, (01)00880304857285(17)310727(10)886210], [886220, (01)00880304857285(17)310726(10)886220], [886230, (01)00880304857285(17)310813(10)886230], [886240, (01)00880304857285(17)310805(10)886240], [886260, (01)00880304857285(17)310922(10)886260], [886270, (01)00880304857285(17)310922(10)886270], [886290, (01)00880304857285(17)310917(10)886290], [954740, (01)00880304857285(17)310922(10)954740], [954760, (01)00880304857285(17)310922(10)954760]

Lot Numbers:
Number
Product: BIOMET Trauma, [Item # 13182-22-26, DVR CROSSLOCK EXTRA LONG PLATE LEFT], [Item # 1318-12-126, DVR CROSSLOCK EXTRA LONG PLATE RIGHT], [Item # 1318-12-176, DVR CROSSLOCK EXTRA EXTRA LONG PLATE RIGHT]. Devices are packaged in a vacuum sealed nylon pouch, which is placed in a carton with the appropriate IFU and patient record labels. Identifying labels on the pouch and the carton.

6 lots: Lot #, UDI - [101220, (01)00887868446191(17)310623(10)101220], [101340, (01)00887868446207(17)310625(10)101340], [101450, (01)00887868446313(17)310630(10)101450], [101560, (01)00887868446191(17)310624(10)101560], [119180, (01)00887868446313(17)310630(10)119180], [154060, (01)00887868446313(17)310630(10)154060]

Product: BIOMET TRAUMA A.L.P.S. FIBULA COMPOSITE LOCKING PLATE 8 HOLE, Item # 856204008. Devices are packaged in a vacuum sealed nylon pouch, which is placed in a carton with the appropriate IFU and patient record labels. Identifying labels on the pouch and the carton.

Lot # 913430, UDI:(01)00887868445897(17)310616(10)913430

Lot Numbers:
913430
Product: BIOMET TRAUMA Drill Bit, Tap, Guide Pin: [DVR Drill Bit, Item # 212000022, DVR 2.2MM DRILL BIT], [ALPS Drill Bit, Item # 214227160, 2.7X160MM CALIBRATED DRILL], [ALPS Drill Bit, Item # 824273100, 4.5X150MM DRILL], [ALPS Drill Bit, Item # 829029170, 2.5X140MM DRILL], [ALPS Drill Bit, Item # 829032170, 3.5X140MM DRILL], [ALPS Tap, Item # 824150170, 3.5X140MM CORTICAL TAP], [ALPS Guide Pin, Item # 829516150, 1.6X150MM BAYONET TIP GUIDE PIN], [ALPS Guide Pin, Item # 829516151, 1.6X150MM THREADED TIP

44 lots: Lot #, UDI # - [014490, (01)00887868447037(17)310608(10)014490], [014500, (01)00887868447068(17)310608(10)014500], [014520, (01)00887868447068(17)310610(10)014520], [084850, (01)00887868447006(17)310621(10)084850], [084860, (01)00887868447006(17)310623(10)084860], [084870, (01)00887868447006(17)310623(10)084870], [084880, (01)00887868447006(17)310624(10)084880], [102920, (01)00887868447006(17)310630(10)102920], [102930, (01)00887868447006(17)310716(10)102930], [102940, (01)00887868447006(17)310729(10)102940], [102950, (01)00887868447006(17)310729(10)102950], [102960, (01)00887868447006(17)310728(10)102960], [103120, (01)00887868447006(17)310728(10)103120], [119750, (01)00887868446054(17)310624(10)119750], [119760, (01)00887868446054(17)310624(10)119760], [120800, (01)00887868446054(17)310630(10)120800], [120810, (01)00887868446054(17)310713(10)120810], [204700, (01)00887868447006(17)310714(10)204700], [205750, (01)00887868447006(17)310714(10)205750], [331580, (01)00887868446054(17)310803(10)331580], [331590, (01)00887868446054(17)310723(10)331590], [331600, (01)00887868446054(17)310726(10)331600], [386440, (01)00887868447105(17)310809(10)386440], [391450, (01)00887868446054(17)310816(10)391450], [391470, (01)00887868447068(17)310811(10)391470], [391660, (01)00887868447068(17)310811(10)391660], [391670, (01)00887868447075(17)310811(10)391670], [416500, (01)00887868446054(17)310817(10)416500], [416510, (01)00887868446054(17)310817(10)416510], [416520, (01)00887868446054(17)310819(10)416520], [416640, (01)00887868446054(17)310823(10)416640], [492660, (01)00887868447006(17)310722(10)492660], [534680, (01)00887868446948(17)310713(10)534680], [534690, (01)00887868446948(17)310713(10)534690], [534700, (01)00887868446948(17)310812(10)534700], [610840, (01)00887868446948(17)310915(10)610840], [806490, (01)00887868447075(17)310528(10)806490], [820340, (01)00887868447006(17)310618(10)820340], [834950, (01)00887868446733(17)311101(10)834950], [836360, (01)00887868446948(17)310119(10)836360], [896640, (01)00887868446733(17)311101(10)896640], [896660, (01)00887868446733(17)311027(10)896660], [939270, (01)00887868447068(17)310601(10)939270], [964360, (01)00887868447068(17)310603(10)964360]

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 89701
Status: Resolved
Manufacturer: Biomet, Inc.
Manufactured In: United States
Units Affected: 4 products (702; 38; 12; 2594)

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AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.