RecallRadar

FDA Device recall Z-2339-2023

Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound Gel

On 2023-08-09 the FDA classified a Class II recall of Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound Gel by Medline Industries Northfield, citing potential for the labeled sterile ultrasound gel component within packs to not meet sterility specifications.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2339-2023
ClassificationClass II
Statusongoing
Initiated2023-05-15
Published2023-08-09
Last updated2026-09-13 11:56 UTC
CompanyMedline Industries Northfield
DistributionUS

Product

Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound Gel. Labeled as the following: a. BREAST BIOPSY KIT, Model Number: DYNDA1224A, DYNDA1224B; b. BREAST BIOPSY TRAY, Model Number: SPEC0130C; c. BREAST IMAGING TRAY, Model Number: MNS11895; d. ULTRASOUND BREAST BIOPSY, Model Number: DYNDH1496; e. ULTRASOUND GUIDE BREAST BIOPSY, Model Number: DYNDH1319; f. US BREAST BIOPSY TRAY, Model Number: DYNDH1187A;

Reason

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

Identifiers

upc10888277985643
upc10193489191448
upc10193489196641
upc10653160324645
upc10193489193947
upc10889942795475
upc10889942702633
code_info
All lot numbers for the following models and corresponding UPCs distributed from Medline between 04/01/2020 and 04/28/2…All lot numbers for the following models and corresponding UPCs distributed from Medline between 04/01/2020 and 04/28/2023: a. Model Number: DYNDA1224A, UPC Number: 10888277985643; Model Number: DYNDA1224B, UPC Number: 10193489191448. b. Model Number: SPEC0130C, UPC Number: 10193489196641. c. Model Number: MNS11895, UPC Number: 10653160324645. d. Model Number: DYNDH1496, UPC Number: 10193489193947. e. Model Number: DYNDH1319, UPC Number: 10889942795475. f. Model Number: DYNDH1187A, UPC Number: 10889942702633.

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2339-2023%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.