Atlas FDA

Material Description (Material Number) 24GA. PENCAN SPINAL BUP. TRAY W/DURAPREP (333867); 25GA. PENCAN SPINAL BUP. TRAY

FDA device recall Z-2276-2026 · posted 2026-06-03 · Open, Classified

Recall details

Recalling firm
B Braun Medical Inc
Reason for recall
A sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. Huon Co, Ltd. has issued a voluntary recall due to potential quality issues.
Action taken
On May 6, 2026, URGENT MEDICAL DEVICE RECALL were sent to customers. Actions to be taken: - Check inventory for affected product and return to B Braun. The return process will begin when B Braun received the Acknowledgement Form.) - If you are a distributor and have further distributed the product, please forward this notice to your consignees. This recall is to be extended to the hospital/healthcare facility level. Should there be any questions, comments, or concerns, please feel free to contact us via email at recalls@bbraunusa.com or via phone at 844-903-6417 Monday through Friday, 8:00am-5:00pm EST.
Root cause
Under Investigation by firm
Status
Open, Classified
Product code
OFU
Quantity affected
582,030 units
Distribution
US Nationwide distribution.
Date initiated
2026-05-06
Date posted
2026-06-03
Location
Bethlehem, PA

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