Data Foundry

Medical device recalls 2016

Spacelabs Healthcare Xhibit Central Station — Class II medical device recall Z-1092-2016

Terminated recall by Spacelabs Healthcare Inc, reported 2016-03-16, distributed in AL, AZ, CA, CO, CT, FL, GA, GU…. The firm has received one report of values for patient height and weight being switched when input at the Xhib

Recall numberZ-1092-2016
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmSpacelabs Healthcare Inc, Snoqualmie, WA, United States
Recall initiated2016-02-26
Classified2016-03-10
Reported by FDA2016-03-16
Terminated2016-10-24
DistributedAL, AZ, CA, CO, CT, FL, GA, GU, IA, ID, IL, IN, KY, LA, MA, MI, MN, MO, MS, MT, NC, NJ, NY, OH, OK, OR, PA, SC, SD, TN, TX, VA, WA, WY
Countries outside the USAF, AR, AU, BH, BO, BR, CA, CH, CL, CN, CO, CR, DE, DO, FR, GB, IN, IR, IT, KW, MA, MX, MY, NL, PA, PE, PH, PL, PY, QA, RO, SA, SG, SV, TH, TN, TR, TT, TW
Model numbers96102

Product

Spacelabs Healthcare Xhibit Central Station, Model 96102 is used to provide clinicians with central monitoring of patient data for those patients connected to networked Spacelabs Healthcare patient monitors and telemetry transmitters.

Reason for recall

The firm has received one report of values for patient height and weight being switched when input at the Xhibit Central Station, Model 96102, causing a bedside monitor Body Surface Area (BSA) calculation to be in error.

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-1092-2016. 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.