17G Wallace Single Lumen Oocyte Recovery Set ONS1733Recalls & reported problems
Coopersurgical, Inc. · 17G Wallace Single Lumen Oocyte Recovery Set, 950 mm tubing (Box of 10) · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 9
- Deaths reported
- 0
- Injuries reported
- 9
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 9 adverse event reports that list this exact device (DI 00888937021073), received between Oct 25, 2023 and May 8, 2025 — classified as 9 injuries.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (5 reports).
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
Most reported problems
Device problems
- Insufficient Device Problem Information5
- Manufacturing, Packaging or Shipping Problem4
Patient problems
- No Clinical Signs, Symptoms or Conditions5
- Perforation4
- Intermenstrual Bleeding1
Recent adverse event reports
The 9 most recent of 9 reports, in the reporter's own words as published by the FDA.
InjuryMay 8, 2025Manufacturing, Packaging or Shipping Problem; Manufacturing, Packaging or Shipping Problem
IT WAS REPORTED THAT DURING OOCYTE RECOVERY ON (B)(6) 2025, THE PATIENT SUFFERED A HEMOPERITONEUM. NO ADDITIONAL INFORMATION AVAILABLE. ONS1733, 17G WALLACE OOCYTE (B)(4).
Patient problems: Perforation
MAUDE report 21987528 ↗InjuryMay 8, 2025Manufacturing, Packaging or Shipping Problem; Manufacturing, Packaging or Shipping Problem
IT WAS REPORTED THAT DURING OOCYTE RECOVERY ON (B)(6) 2025, THE PATIENT SUFFERED A HEMOPERITONEUM. NO ADDITIONAL INFORMATION AVAILABLE. ONS1733, 17G WALLACE OOCYTE (B)(4).
Patient problems: Perforation
MAUDE report 21987521 ↗InjuryMay 8, 2025Manufacturing, Packaging or Shipping Problem; Manufacturing, Packaging or Shipping Problem
IT WAS REPORTED THAT DURING OOCYTE RECOVERY ON (B)(6) 2025, THE PATIENT SUFFERED A HEMOPERITONEUM AND A HEMORRHAGIC VAGINAL BLEED. NO ADDITIONAL INFORMATION AVAILABLE. ONS1733, 17G WALLACE OOCYTE, 2025-04-0000565.
Patient problems: Intermenstrual Bleeding; Perforation
MAUDE report 21987121 ↗InjuryMay 8, 2025Manufacturing, Packaging or Shipping Problem; Manufacturing, Packaging or Shipping Problem
IT WAS REPORTED THAT DURING OOCYTE RECOVERY ON (B)(6) 2025, THE PATIENT SUFFERED A HEMOPERITONEUM. NO ADDITIONAL INFORMATION AVAILABLE. ONS1733,17G WALLACE OOCYTE (B)(4).
Patient problems: Perforation
MAUDE report 21987105 ↗InjuryDec 14, 2023Insufficient Device Problem Information; Insufficient Device Problem Information
PATIENT 1/2 IT WAS REPORTED THAT DURING AN OOCYTE RETRIEVAL, THE PATIENT SUFFERED A HEMOPERITONEUM. ATTEMPTS FOR ADDITIONAL INFORMATION HAVE BEEN MADE, BUT NONE HAS BEEN PROVIDED. ONS1733 17G WALLACE OOCYTE RCVRY (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18331053 ↗InjuryDec 14, 2023Insufficient Device Problem Information; Insufficient Device Problem Information
PATIENT 2/2. IT WAS REPORTED THAT DURING AN OOCYTE RETRIEVAL, THE PATIENT SUFFERED A HEMOPERITONEUM. ATTEMPTS FOR ADDITIONAL INFORMATION HAVE BEEN MADE, BUT NONE HAS BEEN PROVIDED. ONS1733. 17G WALLACE OOCYTE RCVRY 2023-11-0000656.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18331052 ↗InjuryOct 25, 2023Insufficient Device Problem Information; Insufficient Device Problem Information
NO ADDITIONAL INFORMATION IS AVAILABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18007476 ↗InjuryOct 25, 2023Insufficient Device Problem Information; Insufficient Device Problem Information
NO ADDITIONAL INFORMATION IS AVAILABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18007470 ↗InjuryOct 25, 2023Insufficient Device Problem Information; Insufficient Device Problem Information
NO ADDITIONAL INFORMATION IS AVAILABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18007464 ↗
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- Cook G55493William A. Cook Australia Pty. Ltd. · NEEDLE, ASSISTED REPRODUCTION4 reports
- Cook G55477William A. Cook Australia Pty. Ltd. · NEEDLE, ASSISTED REPRODUCTION4 reports
- Cook G55788William A. Cook Australia Pty. Ltd. · NEEDLE, ASSISTED REPRODUCTION2 reports
- Cook G38432William A. Cook Australia Pty. Ltd. · NEEDLE, ASSISTED REPRODUCTION2 reports
- Cook G55797William A. Cook Australia Pty. Ltd. · NEEDLE, ASSISTED REPRODUCTION1 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 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- 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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