FDAMay 15, 2023device

Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound Gel. Labeled as the following: a. CAROTID, Model Number: DYNJ54287A; b. CAROTID PACK, Model Number: DYNJ66190; c. CAROTID SUPPLY, Model Number: DYNJ905622C; d. CAROTID-LF, Model Number: DYNJ901745J; e. CENTRAL LINE INSER...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Potential for the labeled sterile ultrasound gel component within packs to not meet sterility specifications.

What to do

FDA enforcement status: Ongoing

Brands named

medline industries lp northfieldmedlinemedline industries

UPCs

088994276521019348932219019348926350019348960482019348927806019348992392019532707186019348945453019348937418019348995714019348928490019348950213

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound Gel. Labeled as the following: a. CAROTID, Model Number: DYNJ54287A; b. CAROTID PACK, Model Number: DYNJ66190; c. CAROTID SUPPLY, Model Number: DYNJ905622C; d. CAROTID-LF, Model Number: DYNJ901745J; e. CENTRAL LINE INSER... — Recall Details · AllClear