Simulus™ 750Recalls & reported problems
Medtronic, Inc. · ACCY KIT 750 SIMULUS FLEXIBLE RING/BAN · Class 1
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
- Jan 14, 2020Open, Classified
Demonstration Simulus Reusable Sizer Accessory Kits were being incorrectly sourced to customers. The demonstration product (product used within a wet lab) could have come in contact with non-human (porcine) tissue.
Z-1449-2020 · Root cause: Nonconforming Material/Component · FDA record ↗
Other SIZER, HEART-VALVE, PROSTHESIS devices
- Simulus™ 850Medtronic, Inc. · SIZER, HEART-VALVE, PROSTHESIS1 recall0 reports
- NA 905St. Jude Medical, Inc. · SIZER, HEART-VALVE, PROSTHESIS2 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.