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 C
    • SSK (560670)
    • S B H - SPINAL TRAY SSK (560672)
Lot codes and dates

105 of 105 products

Products covered by this recall
#BarcodesProduct as published
1560074
20404696431787304046964317859UDI-DI Primary/Individual Unit of Use: 04046964317873/04046964317859
3Batch Numbers: 0061960383, 0061972565
4Material: 560214
50404696431806104046964318054UDI-DI Primary/Individual Unit of Use: 04046964318061/04046964318054
6Batch Numbers: 0061971346, 0061977782
7Material: 560272
80404696431810804046964318085UDI-DI Primary/Individual Unit of Use: 04046964318108/04046964318085
9Batch Numbers: 0061960367, 0061971330
10Material: 560327
110404696431822104046964318207UDI-DI Primary/Individual Unit of Use: 04046964318221/04046964318207
12Batch Numbers: 0061960420, 0061977751
13Material: 560394
140404696431842904046964318405UDI-DI Primary/Individual Unit of Use: 04046964318429/04046964318405
15Batch Numbers: 0061964747, 0061976985, 0061983313
16Material: 560428
170404696431861004046964318597UDI-DI Primary/Individual Unit of Use: 04046964318610/04046964318597
18Batch Numbers: 0061976150, 0061979927
19Material: 560462
200404696431876404046964318740UDI-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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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 4:06 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.