Medline Industries, Inc. SYNJ10073DRecalls & reported problems
Medline Industries, Inc. · GYN LAPAROSCOPY PACK · 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
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10193489864540), received between Aug 18, 2026 and Aug 18, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Component Missing” (1 report).
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.
Reports received per month
Recalls naming this device
- Feb 11, 2025Class IIOpen, Classified
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/other quality issues have been identified that may pose a risk to patient health.
Z-1447-2025 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
Most reported problems
Device problems
- Component Missing1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 18, 2026Component Missing
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50308360 ↗
Other Gynecological laparoscopic kit devices
- Medline Industries, Inc. DYNJ44864SMedline Industries, Inc. · Gynecological laparoscopic kit4 recalls0 reports
- Medline Industries, Inc. DYNJ909398AMedline Industries, Inc. · Gynecological laparoscopic kit4 recalls0 reports
- Medline Industries, Inc. DYNJ38844NMedline Industries, Inc. · Gynecological laparoscopic kit4 recalls0 reports
- Medline Industries, Inc. DYNJ66298DMedline Industries, Inc. · Gynecological laparoscopic kit3 recalls1 report
- Medline Industries, Inc. DYNJ906926BMedline Industries, Inc. · Gynecological laparoscopic kit3 recalls0 reports
- Medline Industries, Inc. DYNJ49191BMedline Industries, Inc. · Gynecological laparoscopic kit3 recalls0 reports
- Medline Industries, Inc. DYNJ52564DMedline Industries, Inc. · Gynecological laparoscopic kit3 recalls0 reports
- Medline Industries, Inc. CDS920099SMedline Industries, Inc. · Gynecological laparoscopic kit3 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 · each report above links to its original FDA record
- 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.
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