Reported Aug 3, 2022 · Ongoing

Medline Custom procedural kits labeled as follows: a. GP-NEURO PACK, b. KIT NEUR FUS LUM POST, c. KIT PEDI VP SHUNT, d.…

Medline Industries, LP - Spt

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

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: MEDLINE INDUSTRIES, LP - SPT · 1170 S Northpoint Blvd · Waukegan, IL · 60085-6757

Is this the product you have?

  • Medline Custom
  • procedural kits labeled as followsa. GP-NEURO PACK, b. KIT NEUR FUS LUM POST, c. KIT PEDI VP SHUNT, d. KIT STC NEURO SPINE GENERIC, e. MAIN BASIC NEURO, f. MAJOR NEURO PK-LF, g. NEURO, h. NEURO CERVICAL PACK, i. NINOR NEURO PK-LF, j
  • VP SHUNT PACK Model/Catalog NumberModel
  • Numbers
    • a.DYNJ0397191V
    • b. DYKMBNDL138
    • c. DYNJ907374
    • d. DYKMBNDL40A
    • e. DYNJ908260
    • f. DYNJ21243M
    • g. DYNJ904818D
    • DYNJ905194
    • DYNJ904040D
    • DYNJ904040F
    • DYNJ904818C
    • DYNJ905753A
    • h. DYNJ0101287I
    • i. DYNJ21244N
    • j. DYNJ46530J
Lot codes and dates

15 of 15 products

Products covered by this recall
Model / numberProduct as published
DYNJ0397191VLot Numbers: 22CDC076, 22ADB021, 21KDC417, 21KDB423, 21GDA239, 21KDA879
DYKMBNDL138Lot Numbers: 22OBC508, 22DBD203, 22BBT015, 22NBA962, 21GBG761, 21GBS468, 21HBN643, 21JBB951, 21LBL164, 21DBE120, 21FBE311
DYNJ907374Lot Numbers: 22ALA147, 21KLA187, 21LLA436, 21GMB680
DYKMBNDL40ALot Numbers: 22OBF727, 22EBA075, 21LBQ967, 21LBQ968, 22ABL295, 21FBP377, 21GBB010, 21IBD953, 21IBO781, 21JBT126, 21KBX882, 21CBM834, 21FBB095
DYNJ908260Lot Numbers: 22DBE642, 22ABS925, 22OBA019, 21KBX711, 21LBB504
DYNJ21243MLot Numbers: 22OBJ131, 21FBR040, 21HBP246, 21HBP293, 21LBJ604
DYNJ904818DLot Numbers: 22OBM370, 22BBL695, 21JBM657, 21JBX775, 21LBO565, 21LBP608
DYNJ905194Lot Numbers: 19HBK497
DYNJ904040DLot Numbers: 21EBC547, 21FBF247
DYNJ904040FLot Numbers: 22ABP680, 22OBA915, 22OBE643, 21VBB536
DYNJ904818CLot Numbers: 21FBI236, 21HBF322
DYNJ905753ALot Numbers: 22BBD850, 22BBD854, 21FBS310
DYNJ0101287ILot Numbers: 22CDC182, 22BDA782, 21LDA070, 21KDA985, 21EDA767, 21GDC130, 21HDA996
DYNJ21244NLot Numbers: 22NBA715, 22CBS112, 21GBG678, 21IBL346, 21FBF231
DYNJ46530JLot Numbers: 22CBD976, 21JBX562, 21KBG431
Amount recalled
2850 units

This recall covers 8 products

The agency filed one notice per product. You are reading one of them; the other 7 are below.

Where it was sold

  • Nationwide

Why it was recalled

Kits contain leaking bottles of isopropyl alcohol

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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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, 6:55 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.