Reported Dec 4, 2024 · Ongoing

MEDLINE procedure kits labeled as follows

MEDLINE INDUSTRIES, LP - Northfield

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: MEDLINE INDUSTRIES, LP - Northfield · 3 Lakes Dr · Northfield, IL · 60093-2753

Is this the product you have?

MEDLINE procedure kits labeled as follows

74 of 74 products

Products covered by this recall
Model / numberProduct as published
DYNJRA1268BCOMBINED SPINAL AND EPIDURAL
DYNJRA1268CCOMBINED SPINAL AND EPIDURAL
DYNJRA1739AFEMORAL BLOCK TRAY
DYNJRA1739BFEMORAL BLOCK TRAY
DYNJRA186918G CPNB 20G STYLETED CATHETER
DYNJRA9035CONT EPID 18G NDL/20G CATH
DYNJRA9040TRAY 18G CPNB 20G STYLETED
EPIREINF19OCATHETER REINF W/ CONNECT OT
EPIREINF29CCATHETER REINF WITH CONNECTOR
PAIN0384BCONTINUOUS EPIDURAL UPDATED
PAIN1069CCONT EPI 20G W/HUSTEAD
PAIN1271ACONTINUOUS EPIDURAL
PAIN1281BTRAY, CONT EPI 20G NYL W/ HUST
PAIN1317CONTINUOUS EPIDURAL TRAY
PAIN1353B20G CONT. EPID TRAY
PAIN1358CONTINUOUS EPIDURAL TRAY
PAIN1361TRAY, CONT EPI 20G NYL W/ HUST
PAIN1437AJHAC CONT EPIDURAL
PAIN1453BCONTINUOUS EPIDURAL TRAY
PAIN1536AEPIDURAL CATH KIT
Lot codes and dates

74 of 74 products

Products covered by this recall
#BarcodesProduct as published
11019348937048540193489370486DYNJRA1268B, UDI/DI 10193489370485 (each) 40193489370486 (case), Lot Numbers: 20FLA512, 20HLA422, 20ILA296, 20ILA327, 20LLA223, 21ALA087, 21CLA525
21019348990583040193489905831DYNJRA1268C, UDI/DI 10193489905830 (each) 40193489905831 (case), Lot Numbers: 21ELA224, 21ELA333, 21GLA292, 21GLA895, 21HLA924, 21ILA773, 21JLA824, 22ALA237, 22BLA899, 22DLA197, 22DLA409, 22ELA583, 22ELB120, 22FLA820, 22FLB163, 22GLB081, 22HLA566, 22ILA092, 22LLA800, 23DLA368, 23FLA942, 23GLA321, 23HLA910, 23ILA593, 23JLA268
3101934899249540193489924955DYNJRA1739A, UDI/DI 1019348992495 (each) 40193489924955 (case), Lot Numbers: 23CBE392
41019532741123740195327411238DYNJRA1739B, UDI/DI 10195327411237 (each) 40195327411238 (case), Lot Numbers: 23FBL394, 23GBV201, 23HBG282, 23HBG968, 23IBQ191
51019532701881840195327018819DYNJRA1869, UDI/DI 10195327018818 (each) 40195327018819 (case), Lot Numbers: 23CBE391
61088438961844840884389618449DYNJRA9035, UDI/DI 10884389618448 (each) 40884389618449 (case), Lot Numbers: 22GBO435, 22IBI073, 23BBB167, 23BBS677, 23CBL304, 23FBI382
71019348983051440193489830515DYNJRA9040, UDI/DI 10193489830514 (each) 40193489830515 (case), Lot Numbers: 23CBO446, 23DBK742, 23HBG091, 23HBG092
81019532722297040195327222971EPIREINF19O, UDI/DI 10195327222970 (each) 40195327222971 (case), Lot Numbers: 22HBB281, 23EBO266, 23GBA230, 23HBN806, 23HBR131, 23HBY420
91019532711436740195327114368EPIREINF29C, UDI/DI 10195327114367 (each) 40195327114368 (case), Lot Numbers: 22FBU886, 22HBD608, 22KBK655, 22NBE738, 23ABH589, 23DBK772, 23DBN448, 23JBU253
101019348992684240193489926843PAIN0384B, UDI/DI 10193489926842 (each) 40193489926843 (case), Lot Numbers: 23BMC466, 23FMJ516, 23FMJ523, 23FMJ721, 23HMA617, 23LMB080, 23LMC430
11101953273648940195327364893PAIN1069C, UDI/DI 1019532736489 (each) 40195327364893 (case), Lot Numbers: 23ELA637, 23GLA586, 23HLA616, 23JLB208
121019348961920140193489619202PAIN1271A, UDI/DI 10193489619201 (each) 40193489619202 (case), Lot Numbers: 23BLA979
131019532728821140195327288212PAIN1281B, UDI/DI 10195327288211 (each) 40195327288212 (case), Lot Numbers: 22KLA735, 23ALA157
141088827779710940888277797100PAIN1317, UDI/DI 10888277797109 (each) 40888277797100 (case), Lot Numbers: 22GLA179, 22HLB332, 23CLA460, 23DLA279, 23ELB138, 23FLA944, 23GLA948, 23HLB106, 23ILA924, 23JLB213, 23KLB167
151019348933672640193489336727PAIN1353B, UDI/DI 10193489336726 (each) 40193489336727 (case), Lot Numbers: 20ELA452
161019348958674940193489586740PAIN1358, UDI/DI 10193489586749 (each) 40193489586740 (case), Lot Numbers: 22FLB088, 23CLA573
171019348958684840193489586849PAIN1361, UDI/DI 10193489586848 (each) 40193489586849 (case), Lot Numbers: 22FLA642, 22GLA243, 23ILA612, 23JLA051
18101953271351940195327135196PAIN1437A, UDI/DI 1019532713519 (each) 40195327135196 (case), Lot Numbers: 22EBA985, 23ABO995, 23KBH798, 23KBR650
19101953273103840195327310388PAIN1453B, UDI/DI 1019532731038 (each) 40195327310388 (case), Lot Numbers: 22LLB007, 23ALA593, 23BLA987
201019348928858240193489288583PAIN1536A, UDI/DI 10193489288582 (each) 40193489288583 (case), Lot Numbers: 23CLA081

This recall covers 12 products

The agency filed one notice per product. You are reading one of them; the other 11 are below.

Where it was sold

  • Nationwide

Why it was recalled

The connectors may not allow catheters to be inserted as intended if the connector is not in the fully open position.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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By hazard

Other recalls from MEDLINE INDUSTRIES, LP - Northfield

80 in total.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 7:34 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.