Data Foundry

Medical device recalls 2015

Universal Charger Product Usage: The Stryker Universal Battery… — Class III medical device recall Z-1587-2015

Terminated recall by Stryker Instruments Div. of Stryker Corporation, reported 2015-05-13, distributed nationwide. The Stryker Universal Battery Charger is not transmitting usage data to the Stryker Cloud as designed. The fir

Recall numberZ-1587-2015
Product typeMedical device
ClassificationClass III
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmStryker Instruments Div. of Stryker Corporation, Portage, MI, United States
Recall initiated2015-03-25
Classified2015-05-07
Reported by FDA2015-05-13
Terminated2015-07-08
DistributedNationwide (US)
Countries outside the USCA
Quantity223 chargers
Reason classessoftware
Model numbers7110-120-000

Product

Universal Charger Product Usage: The Stryker Universal Battery Charger is designed to be used in conjunction with and provide power to non-sterile and sterile batteries. The Stryker Universal Battery Charger is a four station, modular battery charger intended to charge Stryker handpiece battery packs only. The battery charger has the optional functionality to track device usage data. Usage data is accumulated by Stryker and reports are able to be provided to the customer. For powered surgical instruments.

Reason for recall

The Stryker Universal Battery Charger is not transmitting usage data to the Stryker Cloud as designed. The firm is initiating a software correction to address the issue.

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-1587-2015. 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.