Z-2509-2019Class II

XP-CR Tibial Tray - Interlok 73mm Item # 195274

Name: Z-2509-2019 XP-CR Tibial Tray - Interlok 73mm Item # 195274
Creator: Zimmer Biomet, Inc.
Published: 2019-08-15
License: https://open.fda.gov/license/

Zimmer GmbH / initiated 2019-08-15 / Terminated / root cause: manufacturing process

FDA source

Zimmer Biomet, Inc. began a recall of XP-CR Tibial Tray - Interlok 73mm Item # 195274 on 2019-08-15. FDA classified it as Class II and gives the reason as "The locking bar not fully engaging". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as manufacturing process.

Recall record

Recall number: Z-2509-2019
Classification: Class II
Status: Terminated
Initiated: 2019-08-15
Posted: 2019-09-12
Terminated: 2021-04-16
Recalling firm: Zimmer GmbH
Product: XP-CR Tibial Tray - Interlok 73mm Item # 195274
Product code: JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
Reason for recall: The locking bar not fully engaging
Root cause tag: manufacturing process
FDA root cause: Manufacturing material removal
Action: Risk Manager Responsibilities: 1.Review this notification and ensure that affected personnel are aware of the contents. 2.If you have affected product at your facility, assist your Zimmer Biomet sales representative and quarantine all affected product. Your Zimmer Biomet sales representative will remove the affected product from your facility. 3.Complete Attachment 1 Certificate of Acknowledgement and send to [email protected]. This form will be returned even if you do not have affected products at your facility. 4.Retain a copy of the acknowledgement form with your recall records in the event of a compliance audit of your facilitys documentation. 5.If you have further questions or concerns after reviewing this notice, please call customer service at 574-371-3071 between 8:00 am and 5:00pm EST, Monday through Friday. Calls received outside of call center operating hours will receive a voicemail prompt or be transferred to an on-call representative in the event of an emergency. Alternatively, your questions may be emailed to [email protected]. Surgeon Responsibilities: 1.Review this notification for awareness of the contents. 2.There are no specific patient monitoring instructions related to this recall that are recommended beyond your existing follow-up schedule. 3.A visual and audible confirmation should be made to ensure complete locking bar insertion. 4.Complete Attachment 1 Certificate of Acknowledgement and send to [email protected]. 5.Retain a copy of the acknowledgement form with your recall records in the event of a compliance audit of your facilitys documentation. 6.If you have further questions or concerns after reviewing this notice, please call customer service at 574-371-3071 between 8:00 am and 5:00pm EST, Monday through Friday. Calls received outside of call center operating hours will receive a voicemail prompt or be transferred to an on-
Quantity in commerce: 327 units
Distribution: State NY IN OH MI GA SC FL MO WI MN ND SD NE NJ PA MD IL IA CA VA NC DC WV AR AL MS AL MI WA OR ID LA FL KS TN MA KY OK TX TX CT AZ NV NM MT WY CO UT DC WY Country: KOREA CHINA CANADA AUSTRALIA JAPAN EMEA SWEDEN ITALY
Product codes and lots: Lot Number 553880 590760 663690 553880R 590750 663670 262430 513080 663720 513080R 472990 938180 578980 090230 159280 676320 258090 043920 066220 206850 322110 352860 841550 917740 966760 283230 374810 283240 996010 352850 352850R 429270 851300 383710 041300 585600 076010 469520 578970 599150 600800 600800R 279040 450360 672600 374090 943410 712580 121150 018040 821330 121140 199740 218670 717190 308100 308110 502840 513070 571040 502840R 513070R 571040R

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-2509-2019
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-2503-2019	Class II	Terminated	Voluntary: Firm initiated	2019-09-18	2019-09-12
Z-2504-2019	Class II	Terminated	Voluntary: Firm initiated	2019-09-18	2019-09-12
Z-2505-2019	Class II	Terminated	Voluntary: Firm initiated	2019-09-18	2019-09-12
Z-2506-2019	Class II	Terminated	Voluntary: Firm initiated	2019-09-18	2019-09-12
Z-2507-2019	Class II	Terminated	Voluntary: Firm initiated	2019-09-18	2019-09-12
Z-2508-2019	Class II	Terminated	Voluntary: Firm initiated	2019-09-18	2019-09-12
Z-2509-2019	Class II	Terminated	Voluntary: Firm initiated	2019-09-18	2019-09-12
Z-2510-2019	Class II	Terminated	Voluntary: Firm initiated	2019-09-18	2019-09-12
Z-2511-2019	Class II	Terminated	Voluntary: Firm initiated	2019-09-18	2019-09-12
Z-2512-2019	Class II	Terminated	Voluntary: Firm initiated	2019-09-18	2019-09-12
Z-2513-2019	Class II	Terminated	Voluntary: Firm initiated	2019-09-18	2019-09-12
Z-2514-2019	Class II	Terminated	Voluntary: Firm initiated	2019-09-18	2019-09-12
Z-2515-2019	Class II	Terminated	Voluntary: Firm initiated	2019-09-18	2019-09-12
Z-2516-2019	Class II	Terminated	Voluntary: Firm initiated	2019-09-18	2019-09-12
Z-2517-2019	Class II	Terminated	Voluntary: Firm initiated	2019-09-18	2019-09-12
Z-2518-2019	Class II	Terminated	Voluntary: Firm initiated	2019-09-18	2019-09-12
Z-2519-2019	Class II	Terminated	Voluntary: Firm initiated	2019-09-18	2019-09-12
Z-2520-2019	Class II	Terminated	Voluntary: Firm initiated	2019-09-18	2019-09-12
Z-2521-2019	Class II	Terminated	Voluntary: Firm initiated	2019-09-18	2019-09-12
Z-2522-2019	Class II	Terminated	Voluntary: Firm initiated	2019-09-18	2019-09-12
Z-2523-2019	Class II	Terminated	Voluntary: Firm initiated	2019-09-18	2019-09-12
Z-2524-2019	Class II	Terminated	Voluntary: Firm initiated	2019-09-18	2019-09-12
Z-2525-2019	Class II	Terminated	Voluntary: Firm initiated	2019-09-18	2019-09-12
Z-2526-2019	Class II	Terminated	Voluntary: Firm initiated	2019-09-18	2019-09-12
Z-2527-2019	Class II	Terminated	Voluntary: Firm initiated	2019-09-18	2019-09-12
Z-2528-2019	Class II	Terminated	Voluntary: Firm initiated	2019-09-18	2019-09-12
Z-2529-2019	Class II	Terminated	Voluntary: Firm initiated	2019-09-18	2019-09-12
Z-2530-2019	Class II	Terminated	Voluntary: Firm initiated	2019-09-18	2019-09-12
Z-2531-2019	Class II	Terminated	Voluntary: Firm initiated	2019-09-18	2019-09-12
Z-2532-2019	Class II	Terminated	Voluntary: Firm initiated	2019-09-18	2019-09-12
Z-2533-2019	Class II	Terminated	Voluntary: Firm initiated	2019-09-18	2019-09-12
Z-2534-2019	Class II	Terminated	Voluntary: Firm initiated	2019-09-18	2019-09-12
Z-2535-2019	Class II	Terminated	Voluntary: Firm initiated	2019-09-18	2019-09-12
Z-2536-2019	Class II	Terminated	Voluntary: Firm initiated	2019-09-18	2019-09-12
Z-2537-2019	Class II	Terminated	Voluntary: Firm initiated	2019-09-18	2019-09-12

Product code JWH

K132873Class IIVanguard Xp Knee SystemBiomet, Inc. / cleared 2013-12-11

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-10-07, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)