Data Foundry

Medical device recalls 2017

ATAR Reusable Extension Cable — Class I medical device recall Z-2340-2017

Terminated recall by Oscor, Inc., reported 2017-07-19, distributed in AK, AL, CA, CO, DC, FL, GA, IA…. The Reusable Oscor ATAR extension cables could separate from the connector during use.

Recall numberZ-2340-2017
Product typeMedical device
ClassificationClass I
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmOscor, Inc., Palm Harbor, FL, United States
Recall initiated2017-03-31
Classified2017-07-13
Reported by FDA2017-07-19
Terminated2024-07-15
DistributedAK, AL, CA, CO, DC, FL, GA, IA, ID, IL, IN, KS, KY, MA, MD, ME, MI, MN, MO, MT, NC, NE, NH, NJ, NM, NY, OH, OK, OR, PA, PR, RI, SC, TN, TX, UT, VA, WA, WI, WV
Countries outside the USAT, AW, CA, CL, CR, DE, EE, GB, GT, HK, IQ, KW, MA, NZ, PA, PK, SA, TR
Quantity19,178 units
Lot numbers53912
Model numbers53912

Product

ATAR Reusable Extension Cable, sold under brand names: ATAR Reusable Series, ATAR 53912 Reusable Series, and XI Reusable Series. Model codes: 53912 - MDTS ATAR REUSABLE, 53912A - MDTS ATAR REUSABLE, ATAR MDTS REUSABLE, ATAR-A DARK BLUE REUSABLE, ATAR-MDT REUSABLE, ATAR-MDT2 REUSABLE, ATAR-MDT2S-A, DK BLUE 30CM REUSABLE, ATAR-MDT2S-V WHITE 30CM REUSABLE, ATAR-MDTL REUSABLE, ATAR-MDTR REUSABLE, ATAR-R REUSABLE, ATAR-R T4P REUSABLE, ATAR-R1 REUSABLE, ATAR-RL REUSABLE, ATAR-T REUSABLE, ATAR-V WHITE REUSABLE, ATAR-V2 REUSABLE, XI.A DARK BLUE REUSABLE, XI.MDT REUSABLE, XI.R REUSABLE, XI.V WHITE, REUSEABLE Cable is intended to connect an electrode/lead from a patients or another cable to a diagnostic machine or an external pacemaker

Reason for recall

The Reusable Oscor ATAR extension cables could separate from the connector during use.

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-2340-2017. 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.