Reported Jun 11, 2025 · Ongoing

Medline Kits containing Codman Disposable Perforator 14 mm

MEDLINE INDUSTRIES, LP - Northfield

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: MEDLINE INDUSTRIES, LP - Northfield · 3 Lakes Dr · Northfield, IL · 60093-2753

Is this the product you have?

Medline Kits containing Codman Disposable Perforator 14 mm

9 of 9 products

Products covered by this recall
Model / numberProduct as published
DYNJ59270CRANI ACCESSORY PACK
DYNJ44805MCRANI PACK-LF
CDS982719VCRANIOTOMY CDS982719W DYNJ904168F DYNJ908404B DYNJ908723A DYNJ908723C
DYNJVB91001ACRANIOTOMY #IMF 56646-LF
CDS981888XCRANIOTOMY CDS CDS983467I
DYNJ09882GCRANIOTOMY PACK-LF DYNJ09882I
DYNJ905879GCRANIOTOMY S NASSAU
DYNJ903713KMHC CRANIOTOMY DYNJ903713L
DYNJ902149JPAD CRANIOTOMY
Lot codes and dates

9 of 9 products

Products covered by this recall
Model / numberBarcodesProduct as published
DYNJ592701088827777151240888277771513CRANI ACCESSORY PACK UDI-DI 10888277771512 (ea), 40888277771513 (case) Lots 23JDB683 23JDC548 24ADB783 24HDA822
DYNJ44805M1019532750687240195327506873CRANI PACK-LF UDI-DI 10195327506872 (ea), 40195327506873 (case) Lots 23JBI747 23KBL228 24ABG696 24CBM117 24EBQ114 24GBJ699
DYNJ908723C101953275108314019532751083210195327645090401953276450911019532739572840195327395729101953274105064019532741050710195327403270401953274032711019845900978540198459009786CRANIOTOMY SKU CDS982719V UDI-DI 10195327510831 (ea), 40195327510832 (case) Lots 23KBP461 23LBN381 24ABB119 24BBC547 24BBI145 SKU CDS982719W UDI-DI 10195327645090 (ea), 40195327645091 (case) Lots 24DBS813 SKU DYNJ904168F UDI-DI 10195327395728 (ea), 40195327395729 (case) Lots 24DBU188 SKU DYNJ908404B UDI-DI 10195327410506 (ea), 40195327410507 (case) Lots 23IDB680 23LDB546 24BDB174 24FDA741 24FDB584 24IDA225 24IDA646 24IDA840 SKU DYNJ908723A UDI-DI 10195327403270 (ea), 40195327403271 (case) Lots 23IBO314 23JBC218 24ABK090 UDI-DI 10198459009785 (ea), 40198459009786 (case) Lots 24IBM205 24IBN365 25ABM356
DYNJVB91001A1019532746646640195327466467CRANIOTOMY #IMF 56646-LF UDI-DI 10195327466466 (ea), 40195327466467 (case) Lots 23JLA765 24DLA724 24DLB006 24ELA325
CDS983467I10195327144760401953271447611019532745794540195327457946CRANIOTOMY CDS SKU CDS981888X UDI-DI 10195327144760 (ea), 40195327144761 (case) Lots 24ABT432 24CBD698 24HBH954 24HBP483 24IBG797 25CBF098 UDI-DI 10195327457945 (ea), 40195327457946 (case) Lots 23KDA336
DYNJ09882I10195327574055401953275740561019845905817240198459058173CRANIOTOMY PACK-LF SKU DYNJ09882G UDI-DI 10195327574055 (ea), 40195327574056 (case) Lots 24CBF778 UDI-DI 10198459058172 (ea), 40198459058173 (case) Lots 24HBN426
DYNJ905879G1019532751299640195327512997CRANIOTOMY S NASSAU UDI-DI 10195327512996 (ea), 40195327512997 (case) Lots 23KBI086 23LBH647 23LBH649 24BBU253 24DBV133 24FBE409
DYNJ903713L10195327201579401953272015701019532753121840195327531219MHC CRANIOTOMY SKU DYNJ903713K UDI-DI 10195327201579 (ea), 40195327201570 (case) Lots 23JBK426 UDI-DI 10195327531218 (ea), 40195327531219 (case) Lots 23KBT939 23LBS862 24ABH577 24CBH126 24CBH771
DYNJ902149J1019532755432340195327554324PAD CRANIOTOMY UDI-DI 10195327554323 (ea), 40195327554324 (case) Lots 23KBP275 24ABJ684 24CBF216 24DBI296 24EBD959 24FBF064 24HBK164 24IBN443
Amount recalled
1,853 total

This recall covers 3 products

The agency filed one notice per product. You are reading one of them; the other 2 are below.

Where it was sold

Why it was recalled

Stop using this product now

Affected kits contain recalled Integra Lifesciences Codman Disposable Perforators due to inadequate welds on specific lots. Perforators with inadequate welds may break or separate.

Using this product could cause serious injury, illness or death — stop using it now.

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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, 6:59 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.