Custom Pack, Kit numbers PSS1300, PSS1471(A, PSS1771, PSS2135(A, PSS2135(B, PSS2207, PSS2412(B, PSS2798,…
Medical device recall Z-0165-2017. Published in FDA’s Enforcement Report on Oct 26, 2016.
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 Oct 26, 2016. Copied from openFDA on Oct 20, 2026.
- Class II FDA’s class
- Terminated its status, in FDA’s file
- Nationwide FDA’s word, and 12 states named
- 6526 kits 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 II, the middle of FDA’s three classes.
“Products that might cause a temporary health problem, or pose only a slight threat of a serious nature. Example: a drug that is under-strength but that is not used to treat life-threatening situations.”
openFDA, in plain words, its enforcement report fields.
“Class II is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.”
FDA’s rule, 21 CFR 7.3(m)(2), eCFR.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
What’s wrong with it?
The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140, of the custom AMS kit were recalled because gloves may contain splits or holes compromising sterility.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
Custom Pack, Kit numbers PSS1300, PSS1471(A, PSS1771, PSS2135(A, PSS2135(B, PSS2207, PSS2412(B, PSS2798, PSS2798(A, PSS2798(B, PSS3054, PSS3463, TVS4011NI(J, TVS4028(A, and TVS4070. convenience custom kits used for general surgery in hospital operating room
6526 kits, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
Lot Numbers/ Expiration Dates: 60238 4/27/2014 63592 5/22/2014 61110 5/31/2014 64981 6/6/2014 64360 6/6/2014 63344 6/17/2014 62792 6/18/2014 63990 6/23/2014 61099 8/21/2014 59122 9/20/2014 65818 11/18/2014 72314 11/25/2014 57135 1/21/2015…
Every code shown here, 1,999 characters
Lot Numbers/ Expiration Dates: 60238 4/27/2014 63592 5/22/2014 61110 5/31/2014 64981 6/6/2014 64360 6/6/2014 63344 6/17/2014 62792 6/18/2014 63990 6/23/2014 61099 8/21/2014 59122 9/20/2014 65818 11/18/2014 72314 11/25/2014 57135 1/21/2015 65766 2/26/2015 73492 3/31/2015 59151 4/24/2015 57576 5/8/2015 70776 5/13/2015 58841 5/15/2015 57136 5/25/2015 59700 7/8/2015 60764 8/7/2015 61177 8/12/2015 61496 8/15/2015 59482 8/19/2015 60670 9/12/2015 60618 9/15/2015 60619 9/20/2015 61098 9/27/2015 65575 10/17/2015 65113 10/18/2015 60828 10/27/2015 62788 11/2/2015 61930 11/4/2015 61354 11/6/2015 66242 11/7/2015 65407 11/8/2015 62515 11/10/2015 65328 11/10/2015 65380 11/16/2015 62064 11/18/2015 61734 11/22/2015 63294 11/28/2015 63296 11/28/2015 63350 12/9/2015 63743 12/11/2015 62511 12/25/2015 63037 12/25/2015 63371 12/28/2015 63295 12/28/2015 64672 1/13/2016 63423 1/16/2016 63746 1/22/2016 63751 1/23/2016 61978 1/28/2016 75438 5/18/2016 57063 5/22/2016 71254 5/26/2016 56759 5/31/2016 57500 6/20/2016 75530 6/25/2016 56878 7/5/2016 67109 7/5/2016 68691 7/7/2016 66642 7/11/2016 57583 7/12/2016 67283 7/19/2016 57518 7/21/2016 67771 7/29/2016 68690 7/30/2016 58316 8/13/2016 58533 8/16/2016 58916 8/23/2016 58970 8/23/2016 68245 9/3/2016 69838 9/15/2016 69469 9/20/2016 66608 9/21/2016 70428 9/29/2016 70203 10/21/2016 69728 11/2/2016 68983 11/16/2016 70998 12/17/2016 71524 12/17/2016 72094 12/18/2016 72507 1/10/2017 72343 1/15/2017 70557 1/17/2017 72354 1/20/2017 72864 1/21/2017 73491 1/22/2017 73575 1/27/2017 72972 3/5/2017 73284 3/7/2017 72863 3/15/2017 73094 3/24/2017 72768 3/29/2017 73764 4/18/2017 74120 4/19/2017 73432 5/21/2017 74424 5/22/2017 74838 5/23/2017 76477 7/20/2017 75810 7/22/2017 75363 7/23/2017 74113 7/27/2017 75811 7/28/2017 75818 7/29/2017 78094 8/29/2017 77196 8/30/2017 77752 9/2/2017 78208 9/15/2017 77605 9/19/2017 76282 9/30/2017 77372 10/8/2017 76910 10/24/2017 78629 11/3/2017 78209 11/3/2017 78766 11/9/2017 79083 11/24/2017 78611 1/4/2018 78612 1/9/2018 78115…
FDA’s list runs to 2,071 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.
Nationwide Distribution to California, Florida, Georgia, Illinois, Kansas, Louisiana, Michigan, New Jersey, Nevada, Texas, Virginia, and Wyoming.
The states and territories these words name
- California
- Florida
- Georgia
- Illinois
- Kansas
- Louisiana
- Michigan
- New Jersey
- Nevada
- Texas
- Virginia
- Wyoming
What FDA means by nationwide
“The term “nationwide” is defined to mean the fifty states or a significant portion. Note that subsequent distribution by the consignees to other parties may not be included.”
openFDA, its enforcement report fields.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
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 Apr 22, 2015.
- FDA classified it on Oct 20, 2016.
- FDA’s Enforcement Report published it on Oct 26, 2016.
- FDA terminated it on Oct 25, 2016.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- Windstone Medical Packaging, Inc., of Billings, MT.
- Who began it, in FDA’s words: Voluntary: Firm initiated.
- How the firm first told its customers: Letter.
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 2,071 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
-
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.