Reported Apr 23, 2025 · Ongoing
Medline Convenience kits used for various procedures
MEDLINE INDUSTRIES, LP - Northfield
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: MEDLINE INDUSTRIES, LP - Northfield · 3 Lakes Dr · Northfield, IL · 60093-2753
Is this the product you have?
Medline Convenience kits used for various procedures
8 of 8 products
| Model / number | Product as published |
|---|---|
DYNJ80786 | PERI GYN PACK |
DYNJ21937J | D & C HYSTEROSCOPY PACK |
DYNJ41949B | VAGINAL HYSTERECTOMY WRH-LF |
DYNJ21824R | HYSTER/RESECTOSCOPE #78-RF |
DYNJ67708A | PERI GYN |
DYNJ56417C | HYSTEROSCOPY PACK |
DYNJ51956B | HYSTEROSCOPY PACK CKHA-LF |
DYNJ41949B | VAGINAL HYSTERECTOMY WRH-LF |
- Lot codes and dates
8 of 8 products
Products covered by this recall # Barcodes Product as published 1 1019532769487640195327694877Lot Number: 24IBH305; 2) DYNJ21937J, UDI-DI: 10195327694876(each), 40195327694877(case) 2 1019532712893740195327128938Lot Number: 24JBN378; 3) DYNJ41949B, UDI-DI: 10195327128937(each), 40195327128938(case) 3 1019532710775840195327107759Lot Number: 24JBT902; 4) DYNJ21824R, UDI-DI: 10195327107758(each), 40195327107759(case) 4 1019532703989940195327039890Lot Number: 24JBU465; 5) DYNJ67708A, UDI-DI: 10195327039899(each), 40195327039890(case) 5 1019532746880440195327468805Lot Number: 24JBV636; 6) DYNJ56417C, UDI-DI: 10195327468804(each), 40195327468805(case) 6 1088994259939440889942599395Lot Number: 24KBB818; 7) DYNJ51956B, UDI-DI: 10889942599394(each), 40889942599395(case) 7 1019532712893740195327128938Lot Number: 24KBC171; 8) DYNJ41949B, UDI-DI: 10195327128937(each), 40195327128938(case) 8 Lot Number: 24KBC614 - Amount recalled
- 671 units
This recall covers 34 products
The agency filed one notice per product. You are reading one of them; the other 33 are below.
21 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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