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U.S. Department of Health and Human Services

Class 2 Device Recall Medline Probe Cover Kits

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  Class 2 Device Recall Medline Probe Cover Kits see related information
Date Initiated by Firm May 18, 2023
Date Posted July 20, 2023
Recall Status1 Open3, Classified
Recall Number Z-2191-2023
Recall Event ID 92466
Product Classification Orthopedic tray - Product Code OJH
Product Medline Probe Cover Kits containing sterile Ultrasound Gel, Labeled as the following:
a) CRANIOTOMY CDS-1, Model Number CDS982889I;
b) JOINT INJECTION TRAY, Model Number DYNDH1722;
c) LOWER EXTREMITY PACK-LF, Model Number DYNJ0604434X;
d) ARTHROSCOPY PACK, Model Number DYNJ44322I;
e) SHOULDER ARTHROSCOPY PACK, Model Number DYNJ44348D;
f) SHOULDER ARTHROSCOPY PACK, Model Number DYNJ44348F;
g) IR ARM PACK, Model Number DYNJ50712C;
h) HYBRID PACK, Model Number DYNJ56907D;
i) TUNNEL PACK, Model Number DYNJ58127B;
j) CRANIOTOMY PACK, Model Number DYNJ61749A;
k) CARPAL TUNNEL KIT, Model Number DYNJ63149A;
l) ANGIOGRAPHY PACK, Model Number DYNJ65963A;
m) ARTHROSCOPY PACK, Model Number DYNJ66402;
n) ARTHROSCOPY PACK, Model Number DYNJ66402A;
o) ARTHROSCOPY PACK, Model Number DYNJ66402C;
p) SHOULDER ARTHROSCOPY PACK, Model Number DYNJ66404;
q) SHOULDER ARTHROSCOPY PACK, Model Number DYNJ66404A;
r) SHOULDER ARTHROSCOPY PACK, Model Number DYNJ66404B;
s) ARTHROSCOPY PACK, Model Number DYNJ68997;
t) MURRIETA PACK, Model Number DYNJ69312;
u) MURRIETA PACK, Model Number DYNJ69312A;
v) SHOULDER ARTHROSCOPY PACK, Model Number DYNJ82077;
w) SCO ARTHROSCOPY, Model Number DYNJ906551A;
x) US JOINT KIT, Model Number DYNJRA1944;
y) HIP FRACTURE NERVE BLOCK, Model Number DYNJRA2085;
z) ENS STERILE POUR IMPLANT-LF, Model Number OST011E;
aa) ARTHROGRAM TRAY, Model Number PAIN1524C;
bb) SHOULDER PACK-LF, Model Number PHS41748D;
cc) LOWER EXTREMITY BLOCK PACK-RX, Model Number SPEC0204D;
dd) UPPER EXTREMITY BLOCK PACK-RX, Model Number SPEC0205F;
Code Information all lots within expiry, distributed from Medline between December 2017 - May 2023: a) Model Number CDS982889I, UDI/DI (EA) 10889942208067, UDI/DI (CS) 40889942208068; b) Model Number DYNDH1722, UDI/DI (EA) 10195327132163, UDI/DI (CS) 40195327132164; c) Model Number DYNJ0604434X, UDI/DI (EA) 10889942763801, UDI/DI (CS) 40889942763802; d) Model Number DYNJ44322I, UDI/DI (EA) 10193489530612, UDI/DI (CS) 40193489530613; e) Model Number DYNJ44348D, UDI/DI (EA) 10889942646722, UDI/DI (CS) 40889942646723; f) Model Number DYNJ44348F, UDI/DI (EA) 10193489530650, UDI/DI (CS) 40193489530651; g) Model Number DYNJ50712C, UDI/DI (EA) 10193489870169, UDI/DI (CS) 40193489870160; h) Model Number DYNJ56907D, UDI/DI (EA) 10193489831566, UDI/DI (CS) 40193489831567; i) Model Number DYNJ58127B, UDI/DI (EA) 10193489482799, UDI/DI (CS) 40193489482790; j) Model Number DYNJ61749A, UDI/DI (EA) 10195327063016, UDI/DI (CS) 40195327063017; k) Model Number DYNJ63149A, UDI/DI (EA) 10193489786477, UDI/DI (CS) 40193489786478; l) Model Number DYNJ65963A, UDI/DI (EA) 10193489992052, UDI/DI (CS) 40193489992053; m) Model Number DYNJ66402, UDI/DI (EA) 10193489352016, UDI/DI (CS) 40193489352017; n) Model Number DYNJ66402A, UDI/DI (EA) 10193489840520, UDI/DI (CS) 40193489840521; o) Model Number DYNJ66402C, UDI/DI (EA) 10193489938456, UDI/DI (CS) 40193489938457; p) Model Number DYNJ66404, UDI/DI (EA) 10193489352078, UDI/DI (CS) 40193489352079; q) Model Number DYNJ66404A, UDI/DI (EA) 10193489840537, UDI/DI (CS) 40193489840538; r) Model Number DYNJ66404B, UDI/DI (EA) 10193489941166, UDI/DI (CS) 40193489941167; s) Model Number DYNJ68997, UDI/DI (EA) 10193489874655, UDI/DI (CS) 40193489874656; t) Model Number DYNJ69312, UDI/DI (EA) 10193489929461, UDI/DI (CS) 40193489929462; u) Model Number DYNJ69312A, UDI/DI (EA) 10195327216771, UDI/DI (CS) 40195327216772; v) Model Number DYNJ82077, UDI/DI (EA) 10195327166953, UDI/DI (CS) 40195327166954; w) Model Number DYNJ906551A, UDI/DI (EA) 10195327124083, UDI/DI (CS) 40195327124084; x) Model Number DYNJRA1944, UDI/DI (EA) 10195327133047, UDI/DI (CS) 40195327133048; y) Model Number DYNJRA2085, UDI/DI (EA) 10195327286743, UDI/DI (CS) 40195327286744; z) Model Number OST011E, UDI/DI (EA) 10888277589322, UDI/DI (CS) 40888277589323; aa) Model Number PAIN1524C, UDI/DI (EA) 10195327271602, UDI/DI (CS) 40195327271603; bb) Model Number PHS41748D, UDI/DI (EA) 10193489784794, UDI/DI (CS) 40193489784795; cc) Model Number SPEC0204D, UDI/DI (EA) 10193489302981, UDI/DI (CS) 40193489302982; dd) Model Number SPEC0205F, UDI/DI (EA) 10193489212884, UDI/DI (CS) 40193489212885
Recalling Firm/
Manufacturer		 MEDLINE INDUSTRIES, LP - Northfield
3 Lakes Dr
Northfield IL 60093-2753
For Additional Information Contact Karin Johnson
886-359-1704
Manufacturer Reason
for Recall		 Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams.
FDA Determined
Cause 2		 Device Design
Action Medline distributed their recall notices to their consignees beginning on 05/18/2023 by letter. The notices explained the problem, and the risk and requested the destruction of the products. Distributors were directed to notify their consignees, have the customers document and destroy any affected product, and include your customers quantities on the response form. Beginning on 05/23/2023, Medline issued another notice to a separate group of consignees requesting that the kits be over labeled. Distributors were directed to notify the customers and have them return any affected product to the distributor for collection and return to Medline. Questions: please contact the Recall Department at 866-359-1704
Quantity in Commerce 19940 units
Distribution Worldwide Distribution: US (Nationwide) and OUS (foreign) United Arab Emirates, Singapore, Lebanon, China Qatar, Costa Rica, India, Canada, Panama & Saudi Arabia.
Total Product Life Cycle TPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 The manufacturer has initiated the recall and not all products have been corrected or removed. This record will be updated as the status changes.
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