Reported Nov 26, 2025 · Ongoing

MEDLINE convenience kits labeled as

Medline Industries, LP

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 · 3 Lakes Dr · Northfield, IL · 60093-2753

Is this the product you have?

MEDLINE convenience kits labeled as

53 of 53 products

Products covered by this recall
Model / numberProduct as published
CDS840261ABGENERAL AAA #11-RF
CDS983637ICAROTID ENDARTERECTOMY CDS-LF
CDS983723JPERIPHERAL VASCULAR CDS
CDS983773JACH OPEN HEART
CDS984255KVASCULAR
DYNJ0161262COPEN HEART CHILDRENS PACK-LF
DYNJ0421380PVASCULAR PACK-LF
DYNJ21877WGEN FEM POP #14-RF
DYNJ22350LVASCULAR PACK
DYNJ27432ACGENERAL CAROTID/AV TRAY #15-RF
DYNJ37284KOPEN HEART PACK
DYNJ38175LACH CABG ADD-ON
DYNJ42921GCARDIOVASCULAR PACK
DYNJ43207KCABG PACK-LF
DYNJ43214FHEART DRAPING PACK-LF
DYNJ44847IAAA PACK
DYNJ44857UCASTRO CABG-COMPONENT PACK
DYNJ44869KFISTULA PACK
DYNJ44879KMAJOR VASCULAR LEG-TEAM
DYNJ44886MPERMANENT PACING
Lot codes and dates

53 of 53 products

Products covered by this recall
#BarcodesProduct as published
11019532722812540195327228126Lot Numbers: 23FBF165, 23JBM632. 2) CDS983637I: UDI/DI 10195327228125 (each), 40195327228126 (case)
21019532732782840195327327829Lot Numbers: 23GBU191. 3) CDS983723J: UDI/DI 10195327327828 (each), 40195327327829 (case)
31019532723361740195327233618Lot Numbers: 23FBA013, 23FBH486, 23GBE805. 4) CDS983773J: UDI/DI 10195327233617 (each), 40195327233618 (case)
41019348928860540193489288606Lot Numbers: 23GBT133, 23HBH924, 23HBL135, 23HBV936. 5) CDS984255K: UDI/DI 10193489288605 (each), 40193489288606 (case)
51019532735728340195327357284Lot Numbers: 23KBU348, 24ABB883, 24ABS338. 6) DYNJ0161262C: UDI/DI 10195327357283 (each), 40195327357284 (case)
61019532708427140195327084272Lot Numbers: 23GDB197, 23GDB757. 7) DYNJ0421380P: UDI/DI 10195327084271 (each), 40195327084272 (case)
71019532710454240195327104543Lot Numbers: 23DMI590, 23FMJ656. 8) DYNJ21877W: UDI/DI 10195327104542 (each), 40195327104543 (case)
81019348944525140193489445252Lot Numbers: 23FBT682, 23GBF898, 23IBC645, 24ABR316. 9) DYNJ22350L: UDI/DI 10193489445251 (each), 40193489445252 (case)
91019532710451140195327104512Lot Numbers: 23LBU055, 24BBQ300. 10) DYNJ27432AC: UDI/DI 10195327104511 (each), 40195327104512 (case)
101019532740103040195327401031Lot Numbers: 23EBU150, 23GBF873, 23HBQ650, 23IBB637. 11) DYNJ37284K: UDI/DI 10195327401030 (each), 40195327401031 (case)
111019532722790640195327227907Lot Numbers: 23IBP124, 23KBF938, 24ABS487. 12) DYNJ38175L: UDI/DI 10195327227906 (each), 40195327227907 (case)
121019348998138440193489981385Lot Numbers: 23FLA915, 23ILA168. 13) DYNJ42921G: UDI/DI 10193489981384 (each), 40193489981385 (case)
131019348995292640193489952927Lot Numbers: 23FBU282, 23IBT172. 14) DYNJ43207K: UDI/DI 10193489952926 (each), 40193489952927 (case)
141019348995307740193489953078Lot Numbers: 23EME962. 15) DYNJ43214F: UDI/DI 10193489953077 (each), 40193489953078 (case)
151019532712755840195327127559Lot Numbers: 23EMA158. 16) DYNJ44847I: UDI/DI 10195327127558 (each), 40195327127559 (case)
161019532729806740195327298068Lot Numbers: 23HLA758, 23HLB101, 23LLA759. 17) DYNJ44857U: UDI/DI 10195327298067 (each), 40195327298068 (case)
171019532712765740195327127658Lot Numbers: 23GBI967, 23GBQ950. 18) DYNJ44869K: UDI/DI 10195327127657 (each), 40195327127658 (case)
181019532728223340195327282234Lot Numbers: 23GBI967, 23GBQ950, 23KMC104. 19) DYNJ44879K: UDI/DI 10195327282233 (each), 40195327282234 (case)
191019532712774940195327127740Lot Numbers: 23DBI854, 23EBH319, 23GBT541. 20) DYNJ44886M: UDI/DI 10195327127749 (each), 40195327127740 (case)
201019532712969940195327129690Lot Numbers: 23DBN895, 23EBU129, 23FBQ134, 23GBQ953, 23HBT951. 21) DYNJ50528M: UDI/DI 10195327129699 (each), 40195327129690 (case)
Amount recalled
5133 kits

This recall covers 21 products

The agency filed one notice per product. You are reading one of them; the other 20 are below.

8 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing SafeAir Smoke Evacuation Pencils. Stryker Instruments has expanded the scope of their recall of SafeAir Smoke Evacuation Pencils previously initiated in October 2024, adding an additional 47 lots to the scope of the recall. The initial recall was due to the potential for product to activate without manual input when plugged into a power source or remain active after buttons are released.

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

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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, 7:37 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.