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

Products covered by this recall
Model / numberProduct as published
DYNJ80786PERI GYN PACK
DYNJ21937JD & C HYSTEROSCOPY PACK
DYNJ41949BVAGINAL HYSTERECTOMY WRH-LF
DYNJ21824RHYSTER/RESECTOSCOPE #78-RF
DYNJ67708APERI GYN
DYNJ56417CHYSTEROSCOPY PACK
DYNJ51956BHYSTEROSCOPY PACK CKHA-LF
DYNJ41949BVAGINAL HYSTERECTOMY WRH-LF
Lot codes and dates

8 of 8 products

Products covered by this recall
#BarcodesProduct as published
11019532769487640195327694877Lot Number: 24IBH305; 2) DYNJ21937J, UDI-DI: 10195327694876(each), 40195327694877(case)
21019532712893740195327128938Lot Number: 24JBN378; 3) DYNJ41949B, UDI-DI: 10195327128937(each), 40195327128938(case)
31019532710775840195327107759Lot Number: 24JBT902; 4) DYNJ21824R, UDI-DI: 10195327107758(each), 40195327107759(case)
41019532703989940195327039890Lot Number: 24JBU465; 5) DYNJ67708A, UDI-DI: 10195327039899(each), 40195327039890(case)
51019532746880440195327468805Lot Number: 24JBV636; 6) DYNJ56417C, UDI-DI: 10195327468804(each), 40195327468805(case)
61088994259939440889942599395Lot Number: 24KBB818; 7) DYNJ51956B, UDI-DI: 10889942599394(each), 40889942599395(case)
71019532712893740195327128938Lot Number: 24KBC171; 8) DYNJ41949B, UDI-DI: 10195327128937(each), 40195327128938(case)
8Lot 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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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 6:58 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.