MEDLINE convenience kits labeled as recallZ-0519-2026 · Medline Industries, LP · initiated Sep 30, 2025
Open, Classified
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from Medline Industries, LP or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
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.
FDA root cause category: Under Investigation by firm
What the company is doing
Medline issued an URGENT MEDICAL DEVICE RECALL notice to its consignees on 09/30/2025 and 10/6/2025 via email and mail. The notice explained the issue with the component, potential risk, and requested the following actions: 1. Immediately check stock for the affected item number(s) and the affected lot number(s) listed within the recall portal. Quarantine all affected product. 2. Please use the link and the information found in the notice to complete the response form. Please list the quantity of affected product in inventory on the form. Even if no affected product is in inventory, please complete and submit the form. 3. Upon receipt of the submitted response form, the customer account will receive over-labels to place on affected inventory, with instructions for the customer staff to remove and discard the affected component prior to using the kit. These labels will be provided via FedEx overnight, if applicable. 4. For distributors or those who have resold or transferred this product to another company or individual, you are required by FDA regulations to notify them of this recall communication. Please include your customers quantities on your response form. Upon receipt of your submitted response form, you will receive over-labels to provide to your customers to affix to their affected product. If you have any questions, contact the Recall Department at 866-359-1704 or [email protected].
Recall details
- Recall number
- Z-0519-2026
- Status
- Open, Classified
- Initiated by the company
- Sep 30, 2025
- Posted by the FDA
- Nov 14, 2025
- Recalling firm
- Medline Industries, LP
- Quantity
- 4214 kits
- Product code
- FTN
- Distribution
- US Nationwide distribution.
Product description
MEDLINE convenience kits labeled as: 1) ACH PLASTICS BREAST-LF, REF CDS983639K; 2) BREAST ABD, REF CDS984267J; 3) PLASTIC PACK, REF DYNJ00264M; 4) BREAST ABDOMINOPLASTY MZ PK-LF, REF DYNJ0428947L; 5) BREAST ABDOMINOPLASTY MB PK-LF, REF DYNJ0428947M; 6) AUGMENTATION #87-RF, REF DYNJ27319V; 7) BREAST AUGMENTATION PACK, REF DYNJ33977M; 8) BREAST RECONSTRUCTION-HOULE, REF DYNJ44852M; 9) BREAST PACK, REF DYNJ57527C; 10) TRANSGENDER MASTECTOMY 2, REF DYNJ58257G; 11) ISS MAJOR BREAST PACK, REF DYNJ58668D; 12) CHEST/BREAST PACK, REF DYNJ66495A; 13) MAJOR PLASTICS PACK, REF DYNJ67968B; 14) BREAST PACK, REF DYNJ68464A; 15) BREAST PACK, REF DYNJ68464B; 16) PLASTIC PACK, REF DYNJ83856; 17) PLASTIC PACK, REF DYNJ83856A; 18) PLASTIC PACK, REF DYNJ83856B; 19) BREAST PACK, REF DYNJ84332A; 20) ACH PLASTICS BREAST PK-LF, REF DYNJ85111; 21) BREAST-CHEST, REF DYNJ900294L; 22) PLASTICS MASTECTOMY, REF DYNJ904966C; 23) BREAST PLASTIC, REF DYNJ906638B; 24) BREAST-CHEST, REF DYNJ907141B; 25) BREAST RECONSTRUCTION PACK, REF DYNJ907791B; 26) BREAST RECONSTRUCTION PACK, REF DYNJ907791D; 27) BREAST HERNIA, REF DYNJ908058A; 28) CHEST BREAST KIT, REF DYNJ909203A; 29) PLASTIC, REF DYNJ909410; 30) PLASTIC, REF DYNJ910440; 31) BREAST -LF, REF DYNJ9426113N; 32) GP-PLASTIC BREAST ABD PACK-LF, REF PHS397064007D.
Code information (models, lots, serial numbers)
Show the full code information (7k characters)
REF CDS983639K: UDI/DI 10195327351533 (each), 40195327351534 (case), Lot Number 23FBP157; REF CDS983639K: UDI/DI 10195327351533 (each), 40195327351534 (case), Lot Number 23GBM569; REF CDS984267J: UDI/DI 10193489288872 (each), 40193489288873 (case), Lot Number 23LBN523; REF CDS984267J: UDI/DI 10193489288872 (each), 40193489288873 (case), Lot Number 24BBA266; REF CDS984267J: UDI/DI 10193489288872 (each), 40193489288873 (case), Lot Number 24CBS676; REF CDS984267J: UDI/DI 10193489288872 (each), 40193489288873 (case), Lot Number 24EBM454; REF DYNJ00264M: UDI/DI 10195327418717 (each), 40195327418718 (case), Lot Number 23HMA639; REF DYNJ00264M: UDI/DI 10195327418717 (each), 40195327418718 (case), Lot Number 23HMF507; REF DYNJ0428947L: UDI/DI 10195327329136 (each), 40195327329137 (case), Lot Number 23GMI327; REF DYNJ0428947L: UDI/DI 10195327329136 (each), 40195327329137 (case), Lot Number 23JMC006; REF DYNJ0428947L: UDI/DI 10195327329136 (each), 40195327329137 (case), Lot Number 23LMA065; REF DYNJ0428947L: UDI/DI 10195327329136 (each), 40195327329137 (case), Lot Number 23LMC367; REF DYNJ0428947M: UDI/DI 10195327586683 (each), 40195327586684 (case), Lot Number 24DMF699; REF DYNJ0428947M: UDI/DI 10195327586683 (each), 40195327586684 (case), Lot Number 24EMA236; REF DYNJ27319V: UDI/DI 10195327208127 (each), 40195327208128 (case), Lot Number 23GBI654; REF DYNJ27319V: UDI/DI 10195327208127 (each), 40195327208128 (case), Lot Number 23GBJ925; REF DYNJ27319V: UDI/DI 10195327208127 (each), 40195327208128 (case), Lot Number 23HBZ090; REF DYNJ33977M: UDI/DI 10195327422523 (each), 40195327422524 (case), Lot Number 23HBB046; REF DYNJ44852M: UDI/DI 10195327325220 (each), 40195327325221 (case), Lot Number 23HME689; REF DYNJ57527C: UDI/DI 10195327243470 (each), 40195327243471 (case), Lot Number 23GBA730; REF DYNJ57527C: UDI/DI 10195327243470 (each), 40195327243471 (case), Lot Number 23HBG731; REF DYNJ57527C: UDI/DI 10195327243470 (each), 40195327243471 (case), Lot Number 23HBT208; REF DYNJ57527C: UDI/DI 10195327243470 (each), 40195327243471 (case), Lot Number 23IBG463; REF DYNJ58257G: UDI/DI 10193489968644 (each), 40193489968645 (case), Lot Number 23KMI230; REF DYNJ58257G: UDI/DI 10193489968644 (each), 40193489968645 (case), Lot Number 24BME250; REF DYNJ58257G: UDI/DI 10193489968644 (each), 40193489968645 (case), Lot Number 24DME657; REF DYNJ58668D: UDI/DI 10195327529857 (each), 40195327529858 (case), Lot Number 23LMB473; REF DYNJ58668D: UDI/DI 10195327529857 (each), 40195327529858 (case), Lot Number 24AMH995; REF DYNJ58668D: UDI/DI 10195327529857 (each), 40195327529858 (case), Lot Number 24EMA379; REF DYNJ66495A: UDI/DI 10195327247584 (each), 40195327247585 (case), Lot Number 23DMG612; REF DYNJ66495A: UDI/DI 10195327247584 (each), 40195327247585 (case), Lot Number 23JMD696; REF DYNJ67968B: UDI/DI 10195327418649 (each), 40195327418640 (case), Lot Number 23IMG461; REF DYNJ67968B: UDI/DI 10195327418649 (each), 40195327418640 (case), Lot Number 24BMC283; REF DYNJ68464A: UDI/DI 10195327261665 (each), 40195327261666 (case), Lot Number 23LBN305; REF DYNJ68464A: UDI/DI 10195327261665 (each), 40195327261666 (case), Lot Number 24CBE964; REF DYNJ68464B: UDI/DI 10195327666224 (each), 40195327666225 (case), Lot Number 24DBP960; REF DYNJ83856: UDI/DI 10195327318253 (each), 40195327318254 (case), Lot Number 23GBV076; REF DYNJ83856A: UDI/DI 10195327520830 (each), 40195327520831 (case), Lot Number 23LBD001; REF DYNJ83856B: UDI/DI 10195327600648 (each), 40195327600649 (case), Lot Number 24CBA468; REF DYNJ83856B: UDI/DI 10195327600648 (each), 40195327600649 (case), Lot Number 24CBJ818; REF DYNJ83856B: UDI/DI 10195327600648 (each), 40195327600649 (case), Lot Number 24EBC307; REF DYNJ84332A: UDI/DI 10198459022432 (each), 40198459022433 (case), Lot Number 24EMI031; REF DYNJ85111: UDI/DI 10195327460808 (each), 40195327460809 (case), Lot Number 23JBC629; REF DYNJ900294L: UDI/DI 10195327554071 (each), 40195327554072 (case), Lot Number 24CBI707; REF DYNJ900294L: UDI/DI 10195327554071 (each), 40195327554072 (case), Lot Number 24EBP322; REF DYNJ900294L: UDI/DI 10195327554071 (each), 40195327554072 (case), Lot Number 24IBK581; REF DYNJ904966C: UDI/DI 10195327574000 (each), 40195327574001 (case), Lot Number 24BBI057; REF DYNJ904966C: UDI/DI 10195327574000 (each), 40195327574001 (case), Lot Number 24CBA316; REF DYNJ904966C: UDI/DI 10195327574000 (each), 40195327574001 (case), Lot Number 24DBS660; REF DYNJ906638B: UDI/DI 10195327421410 (each), 40195327421411 (case), Lot Number 23KBW113; REF DYNJ906638B: UDI/DI 10195327421410 (each), 40195327421411 (case), Lot Number 24BBA200; REF DYNJ906638B: UDI/DI 10195327421410 (each), 40195327421411 (case), Lot Number 24CBG796; REF DYNJ906638B: UDI/DI 10195327421410 (each), 40195327421411 (case), Lot Number 24CBL477; REF DYNJ907141B: UDI/DI 10195327450434 (each), 40195327450435 (case), Lot Number 23HBA138; REF DYNJ907141B: UDI/DI 10195327450434 (each), 40195327450435 (case), Lot Number 23LBP102; REF DYNJ907141B: UDI/DI 10195327450434 (each), 40195327450435 (case), Lot Number 24ABO369; REF DYNJ907141B: UDI/DI 10195327450434 (each), 40195327450435 (case), Lot Number 24BBO672; REF DYNJ907141B: UDI/DI 10195327450434 (each), 40195327450435 (case), Lot Number 24CBL486; REF DYNJ907141B: UDI/DI 10195327450434 (each), 40195327450435 (case), Lot Number 24DBM827; REF DYNJ907791B: UDI/DI 10195327185237 (each), 40195327185238 (case), Lot Number 23EBN537; REF DYNJ907791B: UDI/DI 10195327185237 (each), 40195327185238 (case), Lot Number 23EBT257; REF DYNJ907791D: UDI/DI 10195327439859 (each), 40195327439850 (case), Lot Number 23LBK712; REF DYNJ907791D: UDI/DI 10195327439859 (each), 40195327439850 (case), Lot Number 24DBV324; REF DYNJ908058A: UDI/DI 10195327125424 (each), 40195327125425 (case), Lot Number 24CBI553; REF DYNJ908058A: UDI/DI 10195327125424 (each), 40195327125425 (case), Lot Number 24DBI370; REF DYNJ909203A: UDI/DI 10195327363512 (each), 40195327363513 (case), Lot Number 24ABK735; REF DYNJ909203A: UDI/DI 10195327363512 (each), 40195327363513 (case), Lot Number 24DBR411; REF DYNJ909410: UDI/DI 10195327338473 (each), 40195327338474 (case), Lot Number 23FMB748; REF DYNJ909410: UDI/DI 10195327338473 (each), 40195327338474 (case), Lot Number 23FMI603; REF DYNJ909410: UDI/DI 10195327338473 (each), 40195327338474 (case), Lot Number 23LMH380; REF DYNJ909410: UDI/DI 10195327338473 (each), 40195327338474 (case), Lot Number 24BMG608; REF DYNJ909410: UDI/DI 10195327338473 (each), 40195327338474 (case), Lot Number 24DMD838; REF DYNJ910440: UDI/DI 10195327685973 (each), 40195327685974 (case), Lot Number 24EBJ004; REF DYNJ9426113N: UDI/DI 10195327371449 (each), 40195327371440 (case), Lot Number 23KMI086; REF DYNJ9426113N: UDI/DI 10195327371449 (each), 40195327371440 (case), Lot Number 23LMH856; REF PHS397064007D: UDI/DI 10195327454111 (each), 40195327454112 (case), Lot Number 23HDB143.
Devices named in this recall
32 devices in the FDA device registry whose identifier appears in the recall's code information.
- Medline Industries, Inc. DYNJ44852MMedline Industries, Inc. · Plastic surgery and accessories kit4 recalls0 reports
- Medline Industries, Inc. CDS984267JMedline Industries, Inc. · Plastic surgery and accessories kit3 recalls0 reports
- Medline Industries, Inc. DYNJ907791BMedline Industries, Inc. · Plastic surgery and accessories kit3 recalls0 reports
- Medline Industries, Inc. DYNJ58257GMedline Industries, Inc. · Plastic surgery and accessories kit2 recalls0 reports
- Medline Industries, Inc. DYNJ908058AMedline Industries, Inc. · Plastic surgery and accessories kit2 recalls0 reports
- Medline Industries, Inc. DYNJ27319VMedline Industries, Inc. · Plastic surgery and accessories kit2 recalls0 reports
- Medline Industries, Inc. DYNJ57527CMedline Industries, Inc. · Plastic surgery and accessories kit2 recalls0 reports
- Medline Industries, Inc. DYNJ66495AMedline Industries, Inc. · Plastic surgery and accessories kit2 recalls0 reports
- Medline Industries, Inc. DYNJ68464AMedline Industries, Inc. · Plastic surgery and accessories kit2 recalls0 reports
- Medline Industries, Inc. DYNJ83856Medline Industries, Inc. · Plastic surgery and accessories kit2 recalls0 reports
- Medline Industries, Inc. DYNJ0428947LMedline Industries, Inc. · Plastic surgery and accessories kit2 recalls0 reports
- Medline Industries, Inc. DYNJ909410Medline Industries, Inc. · Plastic surgery and accessories kit2 recalls0 reports
- Medline Industries, Inc. CDS983639KMedline Industries, Inc. · Plastic surgery and accessories kit2 recalls0 reports
- Medline Industries, Inc. DYNJ67968BMedline Industries, Inc. · Plastic surgery and accessories kit2 recalls0 reports
- Medline Industries, Inc. DYNJ907791DMedline Industries, Inc. · Plastic surgery and accessories kit2 recalls0 reports
- Medline Industries, Inc. DYNJ907141BMedline Industries, Inc. · Plastic surgery and accessories kit2 recalls0 reports
- Medline Industries, Inc. DYNJ909203AMedline Industries, Inc. · Plastic surgery and accessories kit1 recall0 reports
- Medline Industries, Inc. DYNJ9426113NMedline Industries, Inc. · Plastic surgery and accessories kit1 recall0 reports
- Medline Industries, Inc. DYNJ00264MMedline Industries, Inc. · Plastic surgery and accessories kit1 recall0 reports
- Medline Industries, Inc. DYNJ906638BMedline Industries, Inc. · Plastic surgery and accessories kit1 recall0 reports
- Medline Industries, Inc. DYNJ33977MMedline Industries, Inc. · Plastic surgery and accessories kit1 recall0 reports
- Medline Industries, Inc. PHS397064007DMedline Industries, Inc. · Plastic surgery and accessories kit1 recall0 reports
- Medline Industries, Inc. DYNJ85111Medline Industries, Inc. · Plastic surgery and accessories kit1 recall0 reports
- Medline Industries, Inc. DYNJ83856AMedline Industries, Inc. · Plastic surgery and accessories kit1 recall0 reports
- Medline Industries, Inc. DYNJ58668DMedline Industries, Inc. · Plastic surgery and accessories kit1 recall0 reports
- Medline Industries, Inc. DYNJ900294LMedline Industries, Inc. · Plastic surgery and accessories kit1 recall0 reports
- Medline Industries, Inc. DYNJ904966CMedline Industries, Inc. · Plastic surgery and accessories kit1 recall0 reports
- Medline Industries, Inc. DYNJ0428947MMedline Industries, Inc. · Plastic surgery and accessories kit1 recall0 reports
- Medline Industries, Inc. DYNJ83856BMedline Industries, Inc. · Plastic surgery and accessories kit1 recall0 reports
- Medline Industries, Inc. DYNJ68464BMedline Industries, Inc. · Plastic surgery and accessories kit1 recall0 reports
- Medline Industries, Inc. DYNJ910440Medline Industries, Inc. · Plastic surgery and accessories kit1 recall0 reports
- Medline Industries, Inc. DYNJ84332AMedline Industries, Inc. · Plastic surgery and accessories kit1 recall0 reports
Other products in the same recall event
The FDA groups related products into one recall event (event 97846).
- Z-0511-2026 · Open, ClassifiedMEDLINE convenience kits labeled as LOCAL BASIC, REF DYNJ34418M
- Z-0512-2026 · Open, ClassifiedMEDLINE convenience kits labeled as: CATH LAB PACEMAKER PACK, REF DYNJ59818A
- Z-0513-2026 · Open, ClassifiedMEDLINE convenience kits labeled as: 1) GENERAL AAA #11-RF, REF CDS840261AB; 2) CAROTID ENDARTERECTOMY CDS-LF, REF CDS983637I; 3) PERIPHERAL VASCULAR CDS, REF CDS983723J; 4) A…
- Z-0514-2026 · Open, ClassifiedMEDLINE convenience kits labeled as: 1) CENTRAL LINE PACK, REF DYNJ00281P; 2) FREE FLAP PACK, REF DYNJ68213C.
- Z-0515-2026 · Open, ClassifiedMEDLINE convenience kits labeled as: 1) BREAST BIOPSY PACK-LF, REF DYNJ0160598C; 2) BIOPSY BREAST PACK, REF DYNJ65361A; 3) BREAST BIOPSY/MASTECTOMY, REF DYNJ908839A.
- Z-0516-2026 · Open, ClassifiedMEDLINE convenience kits labeled as: 1) HEAD AND NECK, REF CDS984259O; 2) HEAD AND NECK, REF CDS984259P; 3) MINOR ENT HARPER PACK-LF, REF DYNJ0160700F; 4) MAJOR ENT HARPER PAC…
- Z-0517-2026 · Open, ClassifiedMEDLINE convenience kits labeled as: 1) MAJOR LAPAROTOMY CDS, REF CDS860015W; 2) MAJOR LAPAROTOMY CDS, REF CDS860015X; 3) MINOR LAPAROTOMY CDS, REF CDS860016R; 4) MINOR LAPARO…
- Z-0518-2026 · Open, ClassifiedMEDLINE convenience kits labeled as: PORT INSERTION PACK, REF DYNJ81597
- Z-0520-2026 · Open, ClassifiedMEDLINE convenience kits labeled as: 1) MINOR SINGLE BASIN PACK, REF DYNJ37698L; 2) BASIN PACK, REF DYNJ50123D; 3) MAJOR BASIN PACK, REF DYNJ59816A; 4) OSC BASIN PACK, REF DYN…
- Z-0521-2026 · Open, ClassifiedMEDLINE convenience kits labeled as: 1) GENERAL LAPAROSCOPY, REF CDS930027W; 2) GENERAL MAJOR CDS, REF CDS980245X; 3) BASIC GENERAL CDS, REF CDS980566F; 4) TOTAL KNEE CDS, REF…
- Z-0522-2026 · Open, ClassifiedMEDLINE convenience kits labeled as: 1) BASIC NEURO PACK, REF CDS780202R; 2) ACDF CDS, REF CDS941061M; 3) NEURO PACK-LF, REF DYNJ0038440C; 4) NEURO VP SHUNT/VAGAL NERVE-RF, RE…
- Z-0523-2026 · Open, ClassifiedMEDLINE convenience kits labeled as: 1) MAJOR VAGINAL HARPER PACK-LF, REF DYNJ0161768G; 2) ACH MAJOR VAGINAL PACK, REF DYNJ67757B.
- Z-0524-2026 · Open, ClassifiedMEDLINE convenience kits labeled as: 1) GYN LAPAROSCOPY CDS #34-RF, REF CDS920099S; 2) GYN LAPAROSCOPY CDS-LF, REF CDS983764J; 3) ROBOTIC, REF CDS984262N; 4) ROBOTIC, REF CDS9…
- Z-0525-2026 · Open, ClassifiedMEDLINE convenience kits labeled as: CIRCUMCISION PACK, REF DYNJ16826O
- Z-0526-2026 · Open, ClassifiedMEDLINE convenience kits labeled as: 1) C-SECTION OR 30 CDS, REF CDS820075W; 2) C-SECTION, REF CDS984261J; 3) C-SECTION CDS, REF CDS985282F; 4) C-SECTION PACK, REF DYNJ02577D;…
- Z-0527-2026 · Open, ClassifiedMEDLINE convenience kits labeled as: 1) GYN LAPAROTOMY HARPER PACK-LF, REF DYNJ0160684F; 2) MAJOR LITHOTOMY PACK-LF, REF DYNJ0425778O; 3) MINOR VAGINAL #76-RF, REF DYNJ27434R; …
- Z-0528-2026 · Open, ClassifiedMEDLINE convenience kits labeled as: GP-LEEP PACK-LF, REF PHS396969004F
- Z-0529-2026 · Open, ClassifiedMEDLINE convenience kits labeled as: 1) MINOR EYE TRAY #81, REF DYNJ27466S; 2) MINOR EYE TRAY #81, REF DYNJ27466T.
- Z-0530-2026 · Open, ClassifiedMEDLINE convenience kits labeled as: 1) NEURO CRANIOTOMY CDS #36-RF, REF CDS780119V; 2) BASIC BACK CDS, REF CDS780147N; 3) INSTRUMENTED BACK CDS, REF CDS780148R; 4) NEURO-LAMI…
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 16, 2026. Text above is shown as published by the FDA.
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