FDA Device recall Z-2340-2017
ATAR Reusable Extension Cable, sold under brand names: ATAR Reusable Series, ATAR 53912 Reusable Series, and XI Reusable Series
- FDA Device
- Class I
- terminated
- Published 2017-07-19
On 2017-07-19 the FDA classified a Class I recall of ATAR Reusable Extension Cable, sold under brand names: ATAR Reusable Series, ATAR 53912 Reusable Series, and XI Reusable Series by Oscor, citing the Reusable Oscor ATAR extension cables could separate from the connector during use.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2340-2017 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2017-03-31 |
| Published | 2017-07-19 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Oscor |
| Distribution | AK, 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 |
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
The Reusable Oscor ATAR extension cables could separate from the connector during use.
Identifiers
| code_info | Model Code (Lot #): 53912 - MDTS ATAR REUSABLE (D2-02245 D2-02269 D2-02304 D2-02310 OR-04362 D2-02459 D2-02487 D…Model Code (Lot #): 53912 - MDTS ATAR REUSABLE (D2-02245 D2-02269 D2-02304 D2-02310 OR-04362 D2-02459 D2-02487 D2 02622 D2-02669 D2-02683 D2-02734 D2-02684 D2-02773 D2-02795 D2-02853 D2-02854 D2-02852 D2-02947 D2-02946 D2-02945 OR-04680 D2-03029 D2-02953 D2-03050 D2-03107 OR-04694 D2-03059 D2-03058 D2 03050 OR-04693 D2-03161 D2-03201 D2-03186 D2-03236 D2-03607 D2-03798 D2-03877 D2-03763 D2-03797 D2-03774 D2-03545 D2-03546 D2-03547 D2-03554 D2-03568 D2-03570 D2-03799 D2-03606 D2-03800 D2-03627 D2-03626 D2-03729 D2-03730 D2-03731 D2-03732 D2-03755 D2-03756 D2-03757 D2-03758 D2-03761 D2-03762 D2-03571 D2-03867 D2-03777 D2-03884 D2-03882 D2-03783 D2-03883 D2-03899 D2-03880 D2-03898 D2-03782 D2-03878 D2-03879 D2-03778 D2-03779 D2-03781 D2-03908 D2-03780 D2-03902 D2-03906 D2-03907 D2-03905 D2-03942 D2-03912 D2-03999 D2-04001 D2-03913 D2-02622), 53912A - MDTS ATAR REUSABLE, ATAR MDTS REUSABLE (D2-01835 D2 |
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Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2340-2017%22
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