Breast Augmentation Pack, Kit
Medical device recall Z-0155-2017. 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
- 1498 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?
Breast Augmentation Pack, Kit part number AMS1786, AMS1786(A, AMS2790, AMS3324, AMS3324(A, and PSS3430. convenience custom kits used for general surgery in hospital operating room
1498 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: 59278 10/2/2013 58407 10/14/2013 62436 12/4/2013 62922 12/18/2013 60740 5/20/2014 63467 6/2/2014 62067 6/7/2014 64703 6/10/2014 61619 6/14/2014 64110 6/14/2014 63539 6/29/2014 65271 7/8/2014 65364 7/11/2014…
Every code shown here, 884 characters
Lot numbers/Expiration dates: 59278 10/2/2013 58407 10/14/2013 62436 12/4/2013 62922 12/18/2013 60740 5/20/2014 63467 6/2/2014 62067 6/7/2014 64703 6/10/2014 61619 6/14/2014 64110 6/14/2014 63539 6/29/2014 65271 7/8/2014 65364 7/11/2014 65837 7/31/2014 70246 9/3/2014 70351 9/4/2014 69850 9/7/2014 67400 9/11/2014 69434 9/18/2014 71639 9/18/2014 68310 9/30/2014 72944 10/1/2014 71948 10/9/2014 71949 10/22/2014 65894 2/7/2015 68624 3/12/2015 77600 8/12/2015 76292 8/14/2015 72862 10/5/2015 73989 10/7/2015 67704 12/5/2015 73680 1/3/2016 74974 1/7/2016 76004 1/9/2016 75570 1/17/2016 73628 1/24/2016 73982 2/3/2016 74027 2/24/2016 74377 3/26/2016 75655 3/29/2016 79047 4/5/2016 78542 4/14/2016 78888 4/27/2016 77381 4/30/2016 57192 5/30/2016 57138 6/4/2016 78207 6/20/2016 71656 8/3/2016 75175 8/19/2016 77224 8/23/2016 74582 9/9/2016 78973 10/28/2016 79324 11/16/2016 79137 11/25/2016
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.”
- 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.