Biomet Microfixation, Inc. BD Recalled component is labeled: BD 60ml Syringe Luer-Lok Tip, REF 309653 STERILE. BD Franklin Lakes, NJ 07417 USA Made in USA , www.bd.com. Lots 7298534 Exp 2012-10 and 7334153 Exp 2012-11. Component is found in: TMJ SYSTEM ARTHROSIMPLICITY KIT REF 922070, STERILE PRODUCT, CAUTION: FEDERAL LAW RESTRICTS THIS DEVICE TO SALE BY OR ON THE ORDER OF A PHYSICIAN. DISTRIBUTED BY: BIOMET MICROFIXATION 1520 TRADEPORT DRIVE JACKSONVILLE, FL 32218 USA www.biometmicrofixation.com Kit contains indiv Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
BD Recalled component is labeled: BD 60ml Syringe Luer-Lok Tip, REF 309653 STERILE. BD Franklin Lakes, NJ 07417 USA Made in USA , www.bd.com. Lots 7298534 Exp 2012-10 and 7334153 Exp 2012-11. Component is found in: TMJ SYSTEM ARTHROSIMPLICITY KIT REF 922070, STERILE PRODUCT, CAUTION: FEDERAL LAW RESTRICTS THIS DEVICE TO SALE BY OR ON THE ORDER OF A PHYSICIAN. DISTRIBUTED BY: BIOMET MICROFIXATION 1520 TRADEPORT DRIVE JACKSONVILLE, FL 32218 USA www.biometmicrofixation.com Kit contains indiv
Brand
Biomet Microfixation, Inc.
Lot Codes / Batch Numbers
BP Syringe Codes 7298534, 7334153. Kit Lot #: 1107001, 1107002, 539500, 542870 542880 543090, 554890, 554900, 554920, 554930, 554940, 554950, 554970, 554980, 554990, 555000, 555010, 555020, 555030, 557720, 557730, 557750, 557790, 557800, 557810, 557820, 557830, 560540, 560550, 560560, 577500, 577510, 577520, 577530, 577560, 577590, 577600, 577610, 577620, 577630, 577640, 577650, 577660, 577680, 577690, 637110, 637120, 661250, 661270, 662960, 666880, 667830, 667850, 685230, 685240, 685250, 685260, 685770, 685780, 685790, 685800, 685810, 685820, 554870, 554880, 554910, 554960, 557780, 577540, 577550, 577570, 577580, 637130, 685760, and 698200.
Products Sold
BP Syringe Codes 7298534, 7334153. Kit Lot #: 1107001, 1107002, 539500, 542870 542880 543090, 554890, 554900, 554920, 554930, 554940, 554950, 554970, 554980, 554990, 555000, 555010, 555020, 555030, 557720, 557730, 557750, 557790, 557800, 557810, 557820, 557830, 560540, 560550, 560560, 577500, 577510, 577520, 577530, 577560, 577590, 577600, 577610, 577620, 577630, 577640, 577650, 577660, 577680, 577690, 637110, 637120, 661250, 661270, 662960, 666880, 667830, 667850, 685230, 685240, 685250, 685260, 685770, 685780, 685790, 685800, 685810, 685820, 554870, 554880, 554910, 554960, 557780, 577540, 577550, 577570, 577580, 637130, 685760, and 698200.
Biomet Microfixation, Inc. is recalling BD Recalled component is labeled: BD 60ml Syringe Luer-Lok Tip, REF 309653 STERILE. BD Franklin La due to Biomet Microfixation, Inc. is recalling their OnPoint TMJ Kit (Part Numbers 24-3050, 24-3055) and Arthrosimplicity TMJ Arthocentesis Kit (Part Number. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Biomet Microfixation, Inc. is recalling their OnPoint TMJ Kit (Part Numbers 24-3050, 24-3055) and Arthrosimplicity TMJ Arthocentesis Kit (Part Numbers 922070, 922090, 922075). These two kits contain a BD sterile disposable 60 ml Luer-Lok syringe, Part number 309653 which is under recall by Becton Dickinson (Recall Number Z-2347-2008). Becton Dickinson has determined that unit package seal integ
Recommended Action
Per FDA guidance
Consignees were notified by a combination of telephone, fax, e-mail and certified mail. Questions related to this notice should be directed to Christy Cain at 1-800-874-7711.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AL, CA, CT, FL, GA, HI, IL, IN, IA, KS, LA, MD, MA, MN, MS, MO, NY, NC, OH, PA, SC, TN, TX, UT, VA
Page updated: Jan 10, 2026