Reported Jul 8, 2026 · Ongoing · Updated Sep 16, 2026
Medline Convenience Kits
Medline Industries, LP
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 · 3 Lakes Dr · Northfield, IL · 60093-2753
Is this the product you have?
Medline Convenience Kits
11 of 11 products
| Model / number | Product as published |
|---|---|
| — | PAIN MGMT/ PREF |
PAIN0072L | MED NDL |
PAIN1317 | CONTINUOUS EPIDURAL TRAY |
PAIN1579A | CONTINUOUS EPIDURAL TRAY |
PAIN1885A | CSE TRAY |
PAIN1967A | REINFORCED CATH EPIDURAL TRAY |
PAIN2269 | TRAY,CON EPID,19G REINF OPNTIP |
PAIN2278 | EPIDURAL TRAY |
PAIN2305 | CONTINUOUS EPIDURAL TRAY |
PAIN2334 | CSE TRAY MEDLINE |
SAMPA0147 | PNBT TRAY |
- Lot codes and dates
10 of 10 products
Products covered by this recall # Barcodes Product as published 1 1088827779710940888277797100Lot Number: 25JDB100; 2) PAIN1317, UDI-DI: 10888277797109(each), 40888277797100(case) 2 1019348942244340193489422444Lot Number: 25JLA788; 3) PAIN1579A, UDI-DI: 10193489422443(each), 40193489422444(case) 3 1019532748631040195327486311Lot Number: 25JLA779; 4) PAIN1885A, UDI-DI: 10195327486310(each), 40195327486311(case) 4 1019845924121540198459241216Lot Number: 25JLA861; 5) PAIN1967A, UDI-DI: 10198459241215(each), 40198459241216(case) 5 1019845934200440198459342005Lot Number: 25JLA659; 6) PAIN2269, UDI-DI: 10198459342004(each), 40198459342005(case) 6 1019845937617740198459376178Lot Number: 25JLA781; 7) PAIN2278, UDI-DI: 10198459376177(each), 40198459376178(case) 7 1019845947881940198459478810Lot Number: 25JLA886; 8) PAIN2305, UDI-DI: 10198459478819(each), 40198459478810(case) 8 1019845954063940198459540630Lot Number: 25JLA601; 9) PAIN2334, UDI-DI: 10198459540639(each), 40198459540630(case) 9 1019845955280940198459552800Lot Number: 25JLA942; 10) SAMPA0147, UDI-DI: 10198459552809(each), 40198459552800(case) 10 Lot Number: 25JLA928 - Amount recalled
- 1,512 kits
This recall covers 24 products
The agency filed one notice per product. You are reading one of them; the other 23 are below.
11 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.
This product could cause temporary or reversible health problems — stop using it.
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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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