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Recall Observatory FDA recall evidence

Device product

Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound Gel. Labeled as the following: a. DBD-PACK FETOSCOPY, Model Number: DYNJ906905B; b. FETOSCOPY CDS-LF, Model Number: CDS840215O; c. PACK,FETOSCOPY, Model Number: DYNJ906905A; d. US BREAST BIOPSY TRAY, Model Number: DYNDH1187A;

Z-2310-2023

May 15, 2023

Class II

Product summary

Firm
MEDLINE INDUSTRIES, LP - Northfield
Event
Event 92399
Status
Ongoing
Classification
Class II
Quantity
4,618 kits
Official record key
device-enforcement:Z-2310-2023

Official wording

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

Code information: All lot numbers for the following models and corresponding UPCs distributed from Medline between 04/01/2020 and 04/28/2023: a. Model Number: DYNJ906905B, UPC Number: 019348988494. b. Model Number: CDS840215O, UPC Number: 019348944899. c. Model Number: DYNJ906905A, UPC Number: 019348939112. d. Model Number: DYNDH1187A, UPC Number: 088994270263.

Distribution pattern: Worldwide distribution - US Nationwide and the countries of Canada, China, Costa Rica, India, Lebanon, Panama, Qatar, Saudi Arabia, Singapore, United Arab Emirates.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

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