RecallRadar

FDA Device recall Z-2733-2017

ATAR Disposable Extension Cable, sold under brand names: ATAR Disposable Series, ATAR 53912 Disposable Series, and XI Disposable Series

On 2017-07-19 the FDA classified a Class I recall of ATAR Disposable Extension Cable, sold under brand names: ATAR Disposable Series, ATAR 53912 Disposable Series, and XI Disposable Series by Oscor, citing the Reusable Oscor ATAR extension cables could separate from the connector during use.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2733-2017
ClassificationClass I
Statusterminated
Initiated2017-03-31
Published2017-07-19
Last updated2026-09-13 11:54 UTC
CompanyOscor
DistributionAK, 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 Disposable Extension Cable, sold under brand names: ATAR Disposable Series, ATAR 53912 Disposable Series, and XI Disposable Series. Model codes: ATAR D-A DARK BLUE DISPOSABLE, ATAR D-V WHITE DISPOSABLE, ATAR D-MDT DISPOSABLE, ATAR D-T DISPOSABLE, ATAR D-R DISPOSABLE, ATAR D-RL DISPOSABLE, ATAR D-MDTL DISPOSABLE, ATAR D-MDTS, ATAR D-R1 DISPOSABLE, ATAR D-R NP DISPOSABLE, ATAR D-MDT2, ATAR D-MDTR, ATAR D-R D2P, ATAR D-R T4P, ATAR D-R X2, ATAR D-V2, ATAR D-IS1-2PACE, PACE 101H, PACE 203H WITH ATAR D-MDTS, PACE 203H, PACE 101H WITH ATAR D-T, PACE 300, XI.D-A, DARK BLUE, DISPOSABLE, XI.D-V WHITE DISPOSABLE, XI.D-MDT DISPOSABLE 30 CM, XI.D-T DISPOSABLE, XI.D-RL, XI.D-R DISPOSABLE, 53912D - MDTS ATAR DISPOSABLE 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 #): ATAR D-A DARK BLUE DISPOSABLE (C1-06065 D1-01938-00 D2 01938 D2 02076 D2 02109 D2 02349 D2 02…Model Code (Lot #): ATAR D-A DARK BLUE DISPOSABLE (C1-06065 D1-01938-00 D2 01938 D2 02076 D2 02109 D2 02349 D2 02398 D2 02398. D2 02468 D2 02505 D2 02526 D2 02535 D2 02776 D2 03176 D2 03964 D2 04032 D2-01493 D2-01654 D2-01714 D2-01764 D2-01938 D2-01938-00 D2-02076 D2-02076 00 D2-02109 D2-02136 D2-02194 D2-02349 D2-02389 D2-02398 D2-02398. D2-02468 D2-02468. D2-02503 D2-02505 D202505/2776 D2-02526 D2-02535 D2-02592 D2-02747 D2-02776 D2-02824 D202824/2937 D2-02871 D2-02908 D2-02910 D202910/2994 D2-02915 D2-02916 D2-02934 D2-02936 D2-02937 D2-02977 D2-02994 D2-02995 D2-02996 D2-02997 D2-03039 D2-03043 D2-03051 D2-03057 D2-03092 D2-03124 D2-03136 D203176 D2-03176 D2-03194 D2-03207 D2-03214 D2-03257 D2-03291 D2-03303 D2-03334 D2-03336 D2-03492 D2-03513 D2-03541 D2-03561 D2-03574 D203574/3639 D2-03596 D2-03600 D2-03629 D2-03639 D203639/3652 D2-03652 D2-03690 D2-03691 D2-03694 D2-03695 D2-03698 D2-03741

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-2733-2017%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.