ATAR Reusable Extension Cable
Medical device recall Z-2340-2017. 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
- 19,178 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 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
19,178 units, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
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…
Every code shown here, 1,993 characters
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 D2-02144 D2-02304 D2-02621 D2-02773 D2-02795 D2-03058 D2-02765 D2-03290 D2-03204 D2-03185 D2-03184 D2-03236 D2-03443 D2-02551 D2-02749 D2-03161 D2-02683 D2-02948 D2-03544 D2-02269 OR-04362 D2-02459 D2-02245 D2-03881 D2-01821 D2-03203 D2-03237 D2-03446 D2-03911 DP-02832 D2 02538 DP-03150 OR-04694 D2-03150 D2-03148 D2-03152 D2-03059 D2-03151 D2-03543 D2-03221 D2 03290 D2-03287 D2-03202 D2 03543 D2-03445 D2-03757 D2-03777 D2-03899 D2-03878 D2-03912 D2-03914), ATAR-A DARK BLUE REUSABLE (D2-02776 D2-03741 D2-01574 D8-00030 D2-01779 D8-00011 D2-01779 00 D2-02389 D2 02389 D2-03176 D2-03092 D2-03334 D2-03040 D2-01764 DP-02398 D2-02349 D2-02369 D2-03574 D2 03334 D2-03691 D2-03964 D8-00011-00 D2-02076 D2-02194 D2-03695 D2 01779 D2-01493 D2 02076 D2-02535 D2-03639 D2 01938 D2-01938 00 D2-02503 D2-01938 D2-02359 C1-06065 D2-01654 D2 01714 OR-03910 D2-02109 D2-02526 D2-03600 D2-03629 D2-03652 D2-02824 D2-02398 D2-02468 D2-01679 D2-02937 D2 02468 D2 02503 OR-04391 D2- 02503 D2-02476 OR-04393 D2-01714 D2-01714-0 D2 01779-00 D2 01714-00 D2 02194 OR-04118 D2-03864 D2-01722 D2-02136),…
FDA’s list runs to 4,498 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 4,498 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.