Medline Industries, Inc. DYNJ45334GRecalls & reported problems
Medline Industries, Inc. · MAJOR LAPAROTOMY · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
2 open recalls name this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 2
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
2 FDA recall records name this device's identifier, 2 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Recalls naming this device
- Sep 30, 2025Class IIOpen, Classified
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.
Z-0517-2026 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
- Oct 9, 2024Class IIOpen, Classified
Medline is recalling medical convenience manufactured using certain lots of SafeAir Smoke Evacuation Pencil which were subsequently recalled by Stryker.
Z-0630-2025 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
Other laparoscopy kit devices
- Medline Industries, Inc. DYNJ82871Medline Industries, Inc. · laparoscopy kit5 recalls0 reports
- Medline Industries, Inc. CDS860015WMedline Industries, Inc. · laparoscopy kit4 recalls0 reports
- Medline Industries, Inc. CDS860016RMedline Industries, Inc. · laparoscopy kit4 recalls0 reports
- Medline Industries, Inc. DYNJ0426069NMedline Industries, Inc. · laparoscopy kit4 recalls0 reports
- Medline Industries, Inc. DYNJ905071FMedline Industries, Inc. · laparoscopy kit4 recalls0 reports
- Medline Industries, Inc. DYNJ52656BMedline Industries, Inc. · laparoscopy kit4 recalls0 reports
- Medline Industries, Inc. DYNJ21927RMedline Industries, Inc. · laparoscopy kit4 recalls0 reports
- Medline Industries, Inc. DYNJ58561DMedline Industries, Inc. · laparoscopy kit3 recalls1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page