Medline Industries, Inc. DYNJ52688CRecalls & reported problems
Medline Industries, Inc. · PICC LINE TRAY · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names 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
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 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
- May 18, 2023Class IIOpen, Classified
Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams.
Z-2167-2023 · Root cause: Device Design · Recall details · FDA record ↗
Other Central venous catheter tray devices
- Medline Industries, Inc. DYNJ70141MBMedline Industries, Inc. · Central venous catheter tray4 recalls1 report
- Medline Industries, Inc. DYNJ70152MBMedline Industries, Inc. · Central venous catheter tray4 recalls0 reports
- Medline Industries, Inc. DYNJ80643Medline Industries, Inc. · Central venous catheter tray3 recalls0 reports
- Medline Industries, Inc. DYNJ63199AMedline Industries, Inc. · Central venous catheter tray3 recalls0 reports
- Medline Industries, Inc. DYNJ66271BMedline Industries, Inc. · Central venous catheter tray3 recalls0 reports
- Medline Industries, Inc. DYNJ55546DMedline Industries, Inc. · Central venous catheter tray3 recalls0 reports
- Medline Industries, Inc. DYNJ68037CMedline Industries, Inc. · Central venous catheter tray2 recalls1 report
- Medline Industries, Inc. DYNJ84239Medline Industries, Inc. · Central venous catheter tray2 recalls0 reports
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