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

14 of 14 products

Products covered by this recall
Model / numberProduct as published
DYNJ33638JANGIOGRAM TRAY
DYNJRA1543BLOCK TRAY
DYNJRA1247BMT- NERVE PERIPH PK
DYNJ42367BCVOR ANGIOGRAPHY PACK-LF
DYNJRA1739FEMORAL BLOCK TRAY
DYNJ0134147DNERVE BLOCK ACCESSORY PACK
NERVE BLOCK PREP TRAY, Model Numbers: DYNJRA1220, DYNJRA1571
DYNJRA1109ANERVE BLOCK SUPPORT TRAY
NERVE BLOCK TRAY, Model Numbers: DYNJRA0656A, DYNJRA1287A, DYNJRA1604
DYNJRA0725NERVE BLOCK TRAY/PREFERRED
DYNJ51107BPK, RADIOLOGY-NEURO-IR
DYNJRA1773SINGLE SHOT NERVE BLOCK TRAY
PAIN1622AULTRASOUND BLOCK PREP TRAY
DYNJRA1635AUNIVERSAL BLOCK TRAY/2
Amount recalled
29,126 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.

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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, 5:36 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.