Toomey 188ARecalls & reported problems
Gyrus ACMI, LLC · Toomey Evacuator 50 cc With Adapter · Class 2
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. How this data works · Data updated Oct 13, 2026.
Recalls naming this device
- May 5, 2026Open, Classified
Some sterilization parameters included in the IFU may not consistently render the devices adequately sterile and therefore should no longer be used to sterilize the devices.
Z-2719-2026 · Root cause: Under Investigation by firm · FDA record ↗
Other EVACUATOR, GASTRO-UROLOGY devices
- AHTO 0250070600Stryker Corporation · EVACUATOR, GASTRO-UROLOGY2 recalls44 reports
- Gyrus ACMI 190AGyrus ACMI, LLC · EVACUATOR, GASTRO-UROLOGY2 recalls0 reports
- Gyrus ACMI 194-2Gyrus ACMI, LLC · EVACUATOR, GASTRO-UROLOGY1 recall0 reports
- Toomey 188Gyrus ACMI, LLC · EVACUATOR, GASTRO-UROLOGY1 recall0 reports
- USA Elite 191-NRSGyrus ACMI, LLC · EVACUATOR, GASTRO-UROLOGY1 recall0 reports
- Gyrus ACMI 190-4Gyrus ACMI, LLC · EVACUATOR, GASTRO-UROLOGY1 recall0 reports
- Bard® Ellik Evacuator 000451C. R. Bard, Inc. · EVACUATOR, GASTRO-UROLOGY42 reports
- Urovac Bladder Evacuator M0067301250Boston Scientific Corporation · EVACUATOR, GASTRO-UROLOGY10 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.