ATAR Disposable Extension Cable
Medical device recall Z-2733-2017. Published in FDA’s Enforcement Report on Jul 19, 2017.
- FDA Class I
No Watch here, and no alerts: openFDA asks that its enforcement data “should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall” (openFDA). For FDA’s own recall emails, subscribe at FDA. FDA’s own record is on accessdata.fda.gov.
The short answer
Published in FDA’s Enforcement Report on Jul 19, 2017. Copied from openFDA on Oct 20, 2026.
- Class I FDA’s most serious class (needs attention)
- Terminated its status, in FDA’s file
- 39 states named in where it went
- 36,242 units how much, in FDA’s words
Every line below is in FDA’s own words, with its source beside it. FDA’s terms are explained in FDA’s own words.
How serious is it, by FDA’s class?
Class I, the most serious of FDA’s three classes.
“Dangerous or defective products that predictably could cause serious health problems or death. Examples include: food found to contain botulinum toxin, food with undeclared allergens, a label mix-up on a lifesaving drug, or a defective artificial heart valve.”
openFDA, in plain words, its enforcement report fields.
“Class I is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.”
FDA’s rule, 21 CFR 7.3(m)(1), eCFR.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
What’s wrong with it?
The Reusable Oscor ATAR extension cables could separate from the connector during use.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
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
36,242 units, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
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…
Every code shown here, 2,000 characters
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 D2-03741. D2-03788 D2-03825 D2-03826 D2-03843 D2-03864 D2-03865 D2-03866 D2-03964 D2-04032 D204032/4150 D2-04150 D2-04187 D2-04188 D2-04189 D2-04195 D2-04198 D8-00030 OR-04392 OR-04726), ATAR D-V WHITE DISPOSABLE (D2 02137 D2 02302 D2 02350 D2 02467 D2 02506 D2 02764 D2 03630 D2-01488 D2-01575 D2-01655 D2-01723 D2-01765 D2-01780 D2-02025 D2-02110 D2-02137 D2-02302 D2-02350 D2-02395 D2-02456 D2-02467 D2-02488 D2-02506 D2-02536 D2-02577 D2-02593 D2-02753 D2-02764 D2-02789 D2-02905 D2-02939 D2-02942 D2-03042 D2-03093 D2-03125 D2-03160 D2-03174 D2-03188 D2-03200 D2-03225 D2-03256 D2-03293 D2-03304 D2-03451 D2-03452 D203452/3562 D2-03494 D2-03515 D2-03562 D2-03597 D2-03605 D203630 D2-03630 D2-03640 D2-03692 D2-03693 D2-03696 D2-03700 D2-03742 D2-03743 D2-03767 D203767/3743 D2-03789 D2-03802 D2-03827 D2-03856 D203856/3858 D2-03857 D2-03858 D2-03859 D2-03956 D2-03979 D2-03980 D2-03981 D2-04022 D2-04083 D2-04132 D2-04151 D2-04196 D2-04199 D2-04200 D8-00012 D8-00031 D8-00031-00 DOR01003 DP-02942 OR-03546 OR-04727), ATAR D-MDT DISPOSABLE (D2-02514 D2-02537 D2-02766 D2-02906 D2-02907…
FDA’s list runs to 15,803 characters. The first part is shown; the rest is on FDA’s record.
Copied exactly as FDA lists them: lot and serial numbers, dates and other codes on the product or its label.
Where did it go?
FDA’s words for the “general area of initial distribution”: where the firm first shipped it.
Worldwide Distribution -US to AL, AK, CA, CO, FL, GA, ID, IL, IN, IA , KS, KY, ME, MD, MA, MI, MN, MO, MT, NE, NH, NJ, NM, NY, NC, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, WA, WV, WI, DC. Foreign distribution to following countries: Macedonia, Pakistan, Austria, Canada, Guatemala, United Kingdom, Republic of Panama, Chile, Aruba, Saudi Arabia, Kuwait, Costa Rica, Albania, Estonia, New Zealand, Germany, Puerto Rico, Turkey, Virgin Islands, Iraq, Hong Kong, and Morocco,
The states and territories these words name
39 states and territories.
Every one of them
- Alaska
- Alabama
- California
- Colorado
- District of Columbia
- Florida
- Georgia
- Iowa
- Idaho
- Illinois
- Indiana
- Kansas
- Kentucky
- Massachusetts
- Maryland
- Maine
- Michigan
- Minnesota
- Missouri
- Montana
- North Carolina
- Nebraska
- New Hampshire
- New Jersey
- New Mexico
- New York
- Ohio
- Oklahoma
- Oregon
- Pennsylvania
- Rhode Island
- South Carolina
- Tennessee
- Texas
- Utah
- Virginia
- Washington
- Wisconsin
- West Virginia
The words say it went outside the United States too.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Is it still going on?
Terminated, in FDA’s file.
“FDA has determined that all reasonable efforts have been made to remove or correct the violative product in accordance with the recall strategy, and proper disposition has been made according to the degree of hazard.”
openFDA, on “Terminated”, its enforcement report fields.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
- The firm began the recall on Mar 31, 2017.
- FDA classified it on Jul 13, 2017.
- FDA’s Enforcement Report published it on Jul 19, 2017.
- FDA terminated it on Jul 15, 2024.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- Oscor, Inc., of Palm Harbor, FL.
- Who began it, in FDA’s words: Voluntary: Firm initiated.
- How the firm first told its customers: E-Mail.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
What this record can’t tell you
- Whether your own one is affected: compare the codes, dates and numbers above with yours. When unsure, ask the firm or the store.
- Where it went after the firm’s first shipments. FDA’s words cover the firm’s initial distribution, and, in FDA’s words, “subsequent distribution by the consignees to other parties may not be included.”
- How many have been returned, corrected or destroyed: FDA’s report doesn’t say.
- Whether anyone was hurt or fell ill: the report doesn’t say.
- How current it is: openFDA publishes FDA’s Enforcement Report weekly, after FDA does, and a firm can announce a recall weeks before it appears there. openFDA’s own caution: “This data should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall.”
- FDA’s list of codes runs to 15,803 characters; the first part is shown here, and the rest is on FDA’s record.
- A product with no recall here isn’t safe by that: FDA’s report lists the recalls FDA classified, and when.
Hearth Record wrote these lines; the quotations are FDA’s.
Sources
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U.S. Food and Drug Administration, Device recall enforcement reports.
Released Oct 14, 2026 and checked Oct 20, 2026. Updated weekly. Public domain (CC0 1.0, openFDA). FDA asks that nothing suggest it endorses this site.
Recalls of food, medicines, medical devices, pet food and animal drugs are from the U.S. Food and Drug Administration (FDA). FDA does not endorse Hearth Record. openFDA: “Do not rely on openFDA to make decisions regarding medical care.” Copied on Oct 20, 2026.