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FDA (Device enforcement)Recalled 2023-05-15class ii

MEDLINE INDUSTRIES, LP - Northfield: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound Gel. Labeled as the following: a. CAROTID, Model Number: DYNJ54287A; b. CAROTID PACK,

Hazard

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

Details from the source

Reason for recall: Potential for the labeled sterile ultrasound gel component within packs to not meet sterility specifications. Distribution: Worldwide distribution - US Nationwide and the countries of Canada, China, Costa Rica, India, Lebanon, Panama, Qatar, Saudi Arabia, Singapore, United Arab Emirates. Quantity: 3,431 kits Lot/code info: All lot numbers for the following models and corresponding UPCs distributed from Medline between 04/01/2020 and 04/28/2023: a. Model Number: DYNJ54287A, UPC Number: 088994276521. b. Model Number: DYNJ66190, UPC Number: 019348932219. c. Model Number: DYNJ905622C, UPC Number: 019348926350. d. Model Number: DYNJ901745J, UPC Number: 019348960482. e. Model Number: DYNJ63347A, UPC Number: 019348927806. f. Model Number: CDS983069G, UPC Number: 019348992392. g. Model Number: CDS983069I, UPC Number: 019532707186. h. Model Number: DYNJ47716B, UPC Number: 019348945453. i. Model Number: SYNJ910018A, UPC Number: 019348937418. j. Model Number: DYNJ67954A, UPC Number: 019348995714. k. Model Number: DYNJ65706, UPC Number: 019348928490. l. Model Number: DYNJ905340A, UPC Number: 019348950213. m. Model Number: DYNJ20495J, UPC Number: 019348956435. n. Model Number: DYNJ30245, UPC Number: 008019678769. o. Model Number: DYNJ43861D, UPC Number: 088994276328. p. Model Number: DYNJ63634A, UPC Number: 019532714304. q. Model Number: DYNJ44410F, UPC Number: 019348981154.

UPC codes

088994276521, 019348932219, 019348926350, 019348960482, 019348927806, 019348992392, 019532707186, 019348945453, 019348937418, 019348995714, 019348928490, 019348950213, 019348956435, 008019678769, 088994276328, 019532714304, 019348981154

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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