FDA Device recall Z-2747-2026
MEDLINE ANTERIOR HIP, Medline Kit SKU DYNJ909640G
- FDA Device
- Class I
- ongoing
- Published 2026-07-29
On 2026-07-29 the FDA classified a Class I recall of MEDLINE ANTERIOR HIP, Medline Kit SKU DYNJ909640G by Medline Industries, citing 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. Bra….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2747-2026 |
| Classification | Class I |
| Status | ongoing |
| Initiated | 2026-06-05 |
| Published | 2026-07-29 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Medline Industries |
| Distribution | AZ, CA, FL, IL, IN, NJ, OH, SC |
Product
MEDLINE ANTERIOR HIP, Medline Kit SKU DYNJ909640G
Reason
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. Huons Co, Ltd. has issued a voluntary recall of this product due to quality issues.
Identifiers
| code_info | UDI/DI 10198459280559 (each) 40198459280550 (case), Lot Number 25DBF430 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2747-2026%22
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