PROCEPT BIOROBOTICS CORPORATION recalls
Every recall we track for PROCEPT BIOROBOTICS CORPORATION — 2 in all, from 2019–2021 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
2 recalls since 2017.
All FDA recall records for PROCEPT BIOROBOTICS CORPORATION since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 1 | 0 | 0 | 1 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 1 | 0 | 0 | 1 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled PROCEPT BIOROBOTICS CORPORATION product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All PROCEPT BIOROBOTICS CORPORATION recalls
2 shown- Use cautionMedical device
PROCEPT BIOROBOTICS CORPORATION recalls AQUABEAM Handpiece, REF: HP2000, a sterile single-use component of the AQUABEAM Robotic System.
Procept recalls AQUABEAM HP2000 handpieces due to risk of tip detachment causing procedural delays. Affected units have specific lot numbers. Contact for replacement.
Procept BiometricsJul 9, 2021 - Use cautionMedical device
PROCEPT BIOROBOTICS CORPORATION recalls AquaBeam Handpiece, Sterile EO, Rx Only, REF: 310301, and 320301, a component of AquaBeam Robotic System. 320301
Procept recalls specific lots of AquaBeam Handpiece (REF 310301, 320301) due to potential internal leaks from weld joint cracks. The device may become inoperable with error messages during use.
Procept BiometricsMar 6, 2019
PROCEPT BIOROBOTICS CORPORATION recall questions
How many recalls has PROCEPT BIOROBOTICS CORPORATION had?
2 recalls from PROCEPT BIOROBOTICS CORPORATION are on record with U.S. safety agencies, from 2019–2021.
What is the most recent PROCEPT BIOROBOTICS CORPORATION recall?
PROCEPT BIOROBOTICS CORPORATION recalls AQUABEAM Handpiece, REF: HP2000, a sterile single-use component of the AQUABEAM Robotic System., dated Jul 9, 2021. Every PROCEPT BIOROBOTICS CORPORATION recall is listed on this page, newest first.
What should I do if I have a recalled PROCEPT BIOROBOTICS CORPORATION product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new PROCEPT BIOROBOTICS CORPORATION recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.