Reported Jun 10, 2026 · Ongoing
Design Options Spinal Tray Spinal Needle Anesthesia procedure kits: Material Description (Material Number): SSK H M C…
B Braun Medical Inc.
High riskUsing this product could cause serious injury, illness or death — stop using it now.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: B Braun Medical Inc · 824 12th Ave · Bethlehem, PA · 18018-3524
Is this the product you have?
- Design Options Spinal Tray
- Spinal Needle Anesthesia procedure kitsMaterial
- Description (Material Number)
SSK H M C 20061890 (560074)SSK S C H (560214)SSK BJC H S (ORIGINAL CUST) (560272)SSK CA P M C (ORIGINAL CUST) (560327)SSK T M H (560394)SSK S O 20070208 (560428)SSK L G H (ORIGINAL CUST) (560462)SSK H M H (560465)SSK BUPIVACAINE TRAY 2068824 (560476)SSK K F H (560497)SSK T J U H (560513)SSK O M C (560521)SSK CUSTOM SPINAL TRAY (560523)SSK O R M C (560533)SSK B S H S 20115122 (560538)SSK M M (560572)SSK M S 27GA PENCAN SPINAL TRAY (560580)SSK S T H & C (560584)SSK U C (560587)SSK P25BKG (560603)SSK P24BKG (560606)SSK S25BKG (560607)SSK M C - BUPIVACAINE TRAY (560609)SSK T M C (560613)SSK PENCIL POINT SPINAL TRAY (560619)SSK E O & S H-SPINAL (560621)SSK BSW SPINAL TRAY (560628)SSK M C OB DEPT - SPINAL (560645)SSK B H M (560646)SSK M G M C (560647)SSK S M H (560648)SSK H H S (560660)O S U M C SPINAL TRAY SSK (560667)A M CSSK (560670)S B H - SPINAL TRAY SSK (560672)
- Lot codes and dates
105 of 105 products
Products covered by this recall # Barcodes Product as published 1 560074 2 0404696431787304046964317859UDI-DI Primary/Individual Unit of Use: 04046964317873/04046964317859 3 Batch Numbers: 0061960383, 0061972565 4 Material: 560214 5 0404696431806104046964318054UDI-DI Primary/Individual Unit of Use: 04046964318061/04046964318054 6 Batch Numbers: 0061971346, 0061977782 7 Material: 560272 8 0404696431810804046964318085UDI-DI Primary/Individual Unit of Use: 04046964318108/04046964318085 9 Batch Numbers: 0061960367, 0061971330 10 Material: 560327 11 0404696431822104046964318207UDI-DI Primary/Individual Unit of Use: 04046964318221/04046964318207 12 Batch Numbers: 0061960420, 0061977751 13 Material: 560394 14 0404696431842904046964318405UDI-DI Primary/Individual Unit of Use: 04046964318429/04046964318405 15 Batch Numbers: 0061964747, 0061976985, 0061983313 16 Material: 560428 17 0404696431861004046964318597UDI-DI Primary/Individual Unit of Use: 04046964318610/04046964318597 18 Batch Numbers: 0061976150, 0061979927 19 Material: 560462 20 0404696431876404046964318740UDI-DI Primary/Individual Unit of Use: 04046964318764/04046964318740 - Amount recalled
- 104,720 units
This recall covers 11 products
The agency filed one notice per product. You are reading one of them; the other 10 are below.
Where it was sold
- Nationwide
Why it was recalled
Stop using this product now
These procedure kits contain Bupivacaine Hydrochloride in Dextrose Injection, USP. The manufacturer of the Bupivacaine, Huons Co, Ltd., has issued a voluntary recall due to potential quality issues identified during a recent FDA manufacturing facility inspection.
Using this product could cause serious injury, illness or death — stop using it now.
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