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Medline Anterior Hip Kit
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MEDICAL DEVICE RECALLCRITICAL

Medline Anterior Hip Kit

Medline is recalling anterior hip kits containing Bupivacaine Hydrochloride in Dextrose Injection over quality issues.

What to do

Check whether your kit contains Bupivacaine Hydrochloride in Dextrose Injection, USP, and contact Medline Industries, LP for instructions on returning the affected kit and obtaining a replacement or refund.

Recalled
Listed
Updated
Recall No.
Z-2747-2026
Agency
FDA
Firm
Medline Industries, LP
Recall ID
99290
Status
ONGOING

Why it was recalled

Medline Industries, LP is recalling specific Medline kits containing B. Braun convenience kits that include Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall follows a voluntary recall by Huons Co, Ltd., the manufacturer of the injection, due to quality issues.

Is mine affected?

Check the model, lot, or serial number on the device or its packaging. Yours is affected if it matches one below.

ProductLot codeRecall #UDI-DI
MEDLINE ANTERIOR HIP, Medline Kit SKU DYNJ909640G25DBF430Z-2747-202610198459280559, 40198459280550
MEDLINE convenience kits labeled as25BBC541, 25DBP805Z-2748-202610198459152849, 40198459152840, 10198459252570, 40198459252571
MEDLINE convenience kits labeled as: 1) TOTAL JOINT KIT, Medline Kit SKU DYKS1574A; 2) TOTAL KNEE BASIC, Medline Kit SKU DYNJ902378J; 3) TOTAL HIP, Medline Kit SKU DYNJ903492K; 4) ANTERIOR HIP, Medline Kit SKU DYNJ903493I; 5) ANTERIOR HIP, Medline Kit SKU DYNJ903493J; 6) ANTERIOR HIP, Medline Kit SKU DYNJ903493K; 7) TOTAL HIP, Medline Kit SKU DYNJ906665G; 8) TOTAL KNEE, Medline Kit SKU DYNJ906666J; 9) TOTAL HIP-LF, Medline Kit SKU DYNJ909000A; 10) TOTAL KNEE-LF, Medline Kit–Z-2749-202610198459147449, 40198459147440, 10198459147449, 40198459147440, 10198459128813, 40198459128814, 10198459128813, 40198459128814, 10198459128813, 40198459128814, 10198459128813, 40198459128814, 10198459128813, 40198459128814, 10198459128813, 40198459128814, 10198459255199, 40198459255190, 10198459255199, 40198459255190
MEDLINE convenience kits labeled as25ELB079, 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 (+23 more, see the official notice)–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 (+12 more, see the official notice)

Where it was sold

Distributed in Arizona, California, Florida, Illinois, Indiana, New Jersey, Ohio, and South Carolina.

Timeline

  1. Firm initiated recall
  2. Publicly announced
  3. Listed on Recall Canary
  4. Summary updated

Official source

View on U.S. Food and Drug Administration →

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Editorial summary by Recall Canary · summary updated 2026-09-03 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification