Data Foundry

Medical device recalls 2015

Brand Name: Persona¿ Anterior Referencing Sizer with Locking Boom The… — Class II medical device recall Z-1360-2015

Terminated recall by Zimmer, Inc., reported 2015-04-08, distributed in AL, AZ, CA, CO, FL, GA, HI, IL…. Zimmer, Inc is voluntarily recalling 22 lots of Persona¿ Anterior Referencing Sizer with Locking Boom, part nu

Recall numberZ-1360-2015
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmZimmer, Inc., Warsaw, IN, United States
Recall initiated2015-03-10
Classified2015-04-01
Reported by FDA2015-04-08
Terminated2015-11-06
DistributedAL, AZ, CA, CO, FL, GA, HI, IL, IN, KS, MA, ME, MI, MN, MS, NC, NJ, NY, OH, OK, OR, PA, PR, TN, TX, UT, VA, WI
Countries outside the USCA, DE, DO, IN, JP, KR, SG
Quantity688
Lot numbers56573342, 56574229, 56574230, 56574301, 56574349, 56574374, 56574375, 56574504, 56574505, 56574818, 56574819, 56574820, 56574861, 56574862, 56574863, 56574998, 56574999, 56575000, 56575020, 56575021, 56575072, 56575105
Model numbers42-5099-088-10

Product

Brand Name: Persona¿ Anterior Referencing Sizer with Locking Boom The Persona Anterior Referencing Sizer is a sterilizable instrument intended for use in multiple total knee arthroplasty procedures. The Persona Surgical Technique (97-5026-001-00, Rev. 9) states that the sizer helps ensure that the desired external rotation is attained and provides a size for the femoral component.

Reason for recall

Zimmer, Inc is voluntarily recalling 22 lots of Persona¿ Anterior Referencing Sizer with Locking Boom, part number 42-5099-088-10. Devices are being removed from distribution due to nonconforming to print specifications.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1360-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.