Reported Aug 9, 2023 · Ongoing
Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound Gel. Labeled as the following
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?
Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound Gel. Labeled as the following
8 of 8 products
| Model / number | Product as published |
|---|---|
DYNJ63257C | CUSTOM GYN |
DYNJ906578C | GYN EXP LAPAROTOMY |
DYNJ9048708I | INTRAUTERINE TRNSFUSION -LF |
PHS762887001B | PERI NEURO BLOCK PACK-LF |
DYNJ32988 | PICC TRAY |
DYNJ55361 | SLING PACK-LF, , DYNJ55361A |
OBQ056E | TRANS VAGINAL TRAY (KW01JF) |
TVS4700 | TVS4700 CUSTOM PACK |
- Amount recalled
- 6,340 kits
This recall covers 50 products
The agency filed one notice per product. You are reading one of them; the other 49 are below.
37 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
Potential for the labeled sterile ultrasound gel component within packs to not meet sterility specifications.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
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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