FDA recall, , High risk
Medline Convenience Kits
Huons Co, Ltd. has issued a voluntary recall of this product due to quality issues.
Summary by Recall Canary from the FDA notice
What happened
Medline Industries, LP is issuing a recall for specific Medline kits containing B. Braun convenience kits that include Bupivacaine Hydrochloride in Dextrose Injection, USP. B. Braun Medical Inc. was notified by their supplier, Spectra Medical Devices, LLC of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP.
The affected products include Medline Anterior Hip kits and various Medline convenience kits labeled as C-SECTION, TOTAL JOINT KIT, TOTAL KNEE BASIC, TOTAL HIP, ANTERIOR HIP, TOTAL KNEE, TOTAL HIP-LF, and TOTAL KNEE-LF. The recall began June 5, 2026, and was added to the FDA's Enforcement Report July 22, 2026.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is your kit affected?
Affected if its UDI-DI and lot code are listed under that product.
A UDI-DI is the device identifier printed with the barcode on the device label.
Medline convenience kits
- UDI-DI
- 10198459152849
- 40198459152840
- 10198459252570
- 40198459252571
- Lot code
- 25BBC541
- 25DBP805
- UDI-DI
- 10198459147449
- 40198459147440
- 10198459128813
- 40198459128814
- 10198459255199
- 40198459255190
- 10195327565510
- 40195327565511
- 10198459255052
- 40198459255053
- 10198459293122
- 40198459293123
- 10195327092481
- 40195327092482
- 10195327129590
- 40195327129591
- 10195327428327
- 40195327428328
- 10195327428334
- 40195327428335
- 10198459077364
- 40198459077365
- 10198459248375
- 40198459248376
- 10198459257490
- 40198459257491
- 10198459139321
- 40198459139322
- 10198459257452
- 40198459257453
- 10195327389147
- 40195327389148
- 10198459273209
- 40198459273200
- 10198459527814
- 40198459527815
- 10198459250057
- 40198459250058
- 10198459250040
- 40198459250041
- 10198459250064
- 40198459250065
- 10198459392603
- 40198459392604
- 10198459073335
- 40198459073336
- 10198459089282
- 40198459089283
- 10198459123276
- 40198459123277
- 10198459242335
- 40198459242336
- Lot code
- 25ELB079
- 25DLA930
- 25IBN992
- 25HBS205
- 25DBH984
- 25CBB436
- 25ABR220
- 24LBI991
- 25CBR847
- 25CBE741
- 25ADA380
- 24KDA993
- 25CDA748
- 25CDA157
- 25DDA444
- 25GDA109
- 25FDB471
- 25EDB817
- 25BDA465
- 24LDB209
- 24LDA032
- 24KDB063
- 25ABU735
- 24LBU076
- 25EBN666
- 25DBF470
- 25CBA048
- 25FBH718
- 25EBF688
- 25DBO198
- 25ABL694
- 24KBU683
- 25ABI346
- 24LBR150
- 24LBD242
- 25EBM976
- 25CBJ024
- 25BBA740
- 25EBQ769
- 25CBU372
- 25ABF133
- 24LBD821
- 25FBA422
- 25DBS695
- 25CBV173
- 25CBG902
- 25BBN621
- 25ABV657
- 24LBO734
- 24LBO776
- 25CBF686
- 25JBN131
- 25DBD310
- 25HBR652
- 25DBB386
- 25HBU964
- 25DBH861
- 25DBF544
- 25CBM051
- 25CBU686
- 25CBF765
- 25DBK837
- 25CBN099
Medline Anterior Hip, Medline Kit SKU DYNJ909640G
- UDI-DI
- 10198459280559
- 40198459280550
- Lot code
- 25DBF430
Recall details
- Company began the recall
- Company
- Medline Industries, LPNorthfield, Illinois
- Supplier's recall
- B. Braun Spinal Needle Procedure Kits
- Hazard
- Device defect
- Risk
High risk
There is a reasonable chance that using it could cause serious health problems or death.
FDA Class I recall · How risk is rated
- Event ID
- 99290
- Recall numbers
- Z-2747-2026 to Z-2749-2026
All recalls from Medline Industries, LP
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated
