Erbe USA Inc recalls
Every recall we track for Erbe USA Inc — 4 in all, all from 2026 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
4 recalls since 2017.
All FDA recall records for Erbe USA Inc 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 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 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 | 4 | 0 | 0 | 4 |
Most common reasons for Erbe USA Inc recalls
What to do if you have a recalled Erbe USA Inc 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 Erbe USA Inc recalls
2 shown- Use cautionMedical device
Erbe USA Inc recalls ERBECRYO 2 Cryosurgical Unit Model/Catalog Number: 10402-000
Erbe recalls ERBECRYO 2 Cryosurgical Units with serial numbers up to 11608268. A strong pull on the transfer hose may cause CO2 leakage and cryoprobe rupture.
ErbeJun 26, 2026 - Use cautionMedical device
Erbe USA Inc recalls Flexible Cryoprobe (OD 1.1mm, L1.15mm) w/ oversheath (OD2.6mm, L817mm) REF: 20402-401 STERILE EO. For surgical use
Erbe recalls flexible cryoprobes (OD 1.1mm, L1.15mm) with oversheath (OD2.6mm, L817mm) due to risk of rupture during activation. Affected units include specific UDI and lot numbers.
ErbeFeb 12, 2026
Erbe USA Inc recall questions
How many recalls has Erbe USA Inc had?
4 recalls from Erbe USA Inc are on record with U.S. safety agencies, from 2026.
What is the most recent Erbe USA Inc recall?
Erbe USA Inc recalls ERBECRYO 2 Cryosurgical Unit Model/Catalog Number: 10402-000, dated Jun 26, 2026. Every Erbe USA Inc recall is listed on this page, newest first.
Why are Erbe USA Inc products recalled?
The most common reasons on record: Probes may rupture/burst during activation (3).
What should I do if I have a recalled Erbe USA Inc 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 Erbe USA Inc 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.