Drug recall

Flexible Cryoprobe (OD 1.1mm, L1.15mm) w/ oversheath (OD2.6mm, L817mm) REF: 20402-401 STERILE EO. For surgical…

FDA recall event 98429 · Class I · Erbe USA Inc

Key facts

Event ID 98429
Recall numbers Z-1566-2026, Z-1567-2026, Z-1568-2026
Recalling firm Erbe USA Inc
Product type Devices
Products Flexible Cryoprobe (OD 1.1mm, L1.15mm) w/ oversheath (OD2.6mm, L817mm) REF: 20402-401 STERILE EO. For surgical use, Flexible Cryoprobe (OD 1.7mm, L1.15mm) REF: 20402-410. For surgical use, Flexible Cryoprobe (OD 2.4mm, L1.15mm) REF: 20402-411. For surgical use
Classification Class I
Status Ongoing
Voluntary or mandated Firm Initiated
Reason for recall Probes may rupture/burst during activation
Initiation date Feb 12, 2026
Report date Apr 1, 2026
City Marietta
State GA
Country United States
FEI number 1000140388

At a glance

  • 1–9 Products in this recall
  • 1–9 FDA inspections of this firm (FEI)

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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