Z-2532-2019Class II

Vanguard XP Tibial Tray 71 mm Item # 195249

Name: Z-2532-2019 Vanguard XP Tibial Tray 71 mm Item # 195249
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 Vanguard XP Tibial Tray 71 mm Item # 195249 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-2532-2019
Classification: Class II
Status: Terminated
Initiated: 2019-08-15
Posted: 2019-09-12
Terminated: 2021-04-16
Recalling firm: Zimmer GmbH
Product: Vanguard XP Tibial Tray 71 mm Item # 195249
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-
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 584220 590500 590510 663160 663180 663170 660420 117730 332670 833200 373020 373040 373030 515030 515020 515040 752090 752070 752080 919240 919230 846510 764370 764380 837780 754480 837770 861200 881500 881510 984430 984400 039230 052240 039240 881530 984390 039220 984420 052260 984410 090340 570960

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-2532-2019
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

K122160Class IIVanguard Xp Knee SystemBiomet Manufacturing Corp / cleared 2013-03-20

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)