Flexible Cryoprobe (OD 1.7mm, L1.15mm) REF: 20402-410. For surgical use
USFlexible Cryoprobe (OD 1.7mm, L1.15mm) REF: 20402-410. For surgical use
Recalling Firm: Erbe USA Inc
Grund für den Rückruf / Gefahr
TranslatedProbes may rupture/burst during activation
Produktbeschreibung & Identifikation
TranslatedFlexible Cryoprobe (OD 1.7mm, L1.15mm) REF: 20402-410. For surgical use
Betroffene Produkte
TranslatedFlexible Cryoprobe (OD 1.7mm, L1.15mm) REF: 20402-410. For surgical use
Additional Source Details
| Field | Value |
|---|---|
| City | Marietta |
| State | GA |
| Event id | 98429 |
| Address 1 | 2225 Northwest Pkwy SE |
| Code info | UDI: 04050147021822/Expanded Lots: WO472495 WO472496 WO472497 WO472612 WO472613 WO472614 WO473666 WO473667 WO473668 WO473669 WO473670 WO473791 WO476977 WO476978 WO476979 WO476980 WO477011 WO477012 WO477031 WO477511 WO477512 WO477661 WO477662 WO477663 WO477664 WO478276 WO478277 WO478278 WO478279 WO478313 WO478845 WO478846 WO479954 WO479955 WO479956 WO480079; Initial Lots: WO459860 WO462187 WO462322 WO462390 WO462391 WO462392 WO462393 WO462396 WO462677 WO462678 WO463323 WO463324 WO463325 WO463326 WO463386 WO463387 WO464280 WO464281 WO464282 WO464283 WO464284 WO465059 WO465060 WO465061 WO465062 WO467876 WO467877 WO467878 WO467879 WO468225 WO468226 WO468227 WO468642 WO468643 WO468644 WO468645 WO468647 WO468671 WO468672 WO468673 WO468674 WO469361 WO469362 WO469363 W2459858 W2459958 W2462283 W2463593 W2465596 W2465623 W2465693 W2465768 W2468859 W2470050 W2470051 W2470052 W4465597 |
| Postal code | 30067-8764 |
| Report date | 20260401 |
| Product type | Devices |
| Product quantity | 8,284 units |
| Reason for recall | Probes may rupture/burst during activation |
| Voluntary mandated | Voluntary: Firm initiated |
| Recall initiation date | 20260212 |
| Initial firm notification | |
| Center classification date | 20260320 |
Consumer Action Protocol: What You Should Do Immediately
Safety StepsInspect the NDC code, batch number, or control number on your medicine bottle or blister packaging to confirm whether your unit is included.
Do not abruptly stop critical prescribed medication without physician advice. Contact your dispensing pharmacist immediately for a safe alternative.
Under statutory consumer protection rules, consumers are entitled to a full refund, certified replacement, or free repair kit without needing the original sales receipt.
If you suffered an injury, illness, or property damage from this product, file an official incident report with regulatory authorities (FDA Devices).
Your Legal Rights as a Consumer
Recalls are legally binding corrective safety actions overseen by statutory government bodies. Recalling entities are legally prohibited from charging consumers for official safety remedies. If a retailer or dealership refuses your recall remedy, notify the issuing regulatory agency immediately.
Frequently Asked Questions About This Recall
FAQ GuideQ1:What should I do immediately if I own or bought Flexible Cryoprobe (OD 1.7mm, L1.15mm) REF: 20402-410. For surgical use?
Check the lot number and NDC on your prescription label. For essential medications, consult your doctor or dispensing pharmacist immediately before abruptly stopping your dose.
Q2:Can I get a full refund or free repair for this recall?
Yes. Recalling manufacturers and retail merchants are required under consumer protection regulations to offer a statutory remedy—typically a full refund, certified repair kit, or replacement unit.
Q3:Do I need my original sales receipt to claim a remedy or refund?
In most recall cases, no receipt is required. Because safety recalls are matters of public health and statutory compliance, retailers and manufacturers routinely issue refunds, store credit, or replacement kits upon presentation of the affected product or lot code.
Q4:Where can I verify official information for this safety alert?
This safety alert is aggregated directly from official regulatory agency records (FDA Devices). You can click the 'Official Agency Alert' link on this page to view the primary government notice and contact the manufacturer directly.
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Übersicht
- Rückrufendes UnternehmenErbe USA Inc
- StatusOngoing
- RisikostufeClass I
- DistributionUS Nationwide distribution, including Puerto Rico.
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🚨 SAFETY ALERT: Erbe USA Inc - Flexible Cryoprobe (OD 1.7mm, L1.15mm) REF: 20402-410. For surgical use Check if your household is affected: https://therecallfile.com/de/recalls/flexible-cryoprobe-od-1-7mm-l1-15mm-ref-20402-410-for-surgical-use/FDA-Z-1567-2026
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