McKesson 68-102800Recalls & reported problems
Mckesson Medical-Surgical Inc. · DISINFECTANT, GLUTARALDEHYDE · Class 2
Data updated Oct 16, 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 16, 2026.
Recalls naming this device
- May 25, 2022Open, Classified
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.
Z-1614-2022 · Root cause: Environmental control · Recall details · FDA record ↗
Other Sterilant, Medical Devices devices
- Revital-Ox Resert 4455AWSteris Corporation · Sterilant, medical devices1 recall3 reports
- McKesson 341Mckesson Medical-Surgical Inc. · Sterilant, Medical Devices1 recall0 reports
- MetriCide28 10-2800Metrex Research, LLC · Sterilant, medical devices1 recall0 reports
- McKesson 68-101400Mckesson Medical-Surgical Inc. · Sterilant, Medical Devices1 recall0 reports
- MetriCide 10-1400Metrex Research, LLC · Sterilant, medical devices1 recall0 reports
- CIDEX™ 20390Advanced Sterilization Products Services Inc. · Sterilant, medical devices33 reports
- Rapicide High Level Disinfectant and Sterilant ML02-0059Medivators Inc. · Sterilant, Medical Devices6 reports
- SYSTEM 1 endoCorporation Steris Canada · Sterilant, medical devices5 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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