FDA Device recall Z-2748-2026
MEDLINE convenience kits labeled as: 1) C-SECTION, Medline SKU DYNJ910835
- FDA Device
- Class I
- ongoing
- Published 2026-07-29
On 2026-07-29 the FDA classified a Class I recall of MEDLINE convenience kits labeled as: 1) C-SECTION, Medline SKU DYNJ910835 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-2748-2026 |
| 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 convenience kits labeled as: 1) C-SECTION, Medline SKU DYNJ910835; 2) C-SECTION, Medline SKU DYNJ910835A; medical convenience kits
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 | 1) Medline SKU DYNJ910835: 10198459152849 (each) 40198459152840 (case) Kit Lot Number 25BBC541; 2) Medline SKU DYNJ91…1) Medline SKU DYNJ910835: 10198459152849 (each) 40198459152840 (case) Kit Lot Number 25BBC541; 2) Medline SKU DYNJ910835A: 10198459252570 (each) 40198459252571 (case), Kit Lot Number 25DBP805. |
|---|
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-2748-2026%22
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