Device recalls

ERBECRYO 2 Cryosurgical Unit Model/Catalog Number: 10402-000

Erbe USA Inc · A strong pull on the high-pressure transfer hose of cryosurgical unit may lead to pneumatic short circuit between he gas inlet and the connector resulting in C…

Open, ClassifiedDevice DesignZ-2938-2026
Open FDA's page for this record
Cfres ID
221364
Product res number
Z-2938-2026
Event date initiated
2026-06-26
Event date posted
2026-08-12
Recall status
Open, Classified
Res event number
99341
Product code
GEH
Product description
ERBECRYO 2 Cryosurgical Unit Model/Catalog Number: 10402-000
Code info
UDI-DI 04050147013797/ Serial Numbers: All serial numbers up to 11608268 Software Version: 1.0.3
Firm FEI number
1000140388
Recalling firm
Erbe USA Inc
Address 1
2225 Northwest Pkwy SE
City
Marietta
State
GA
Postal code
30067-8764
Additional info contact
Customer Service 770-955-4400 Ext. 133
Root cause description
Device Design
Product quantity
11226 units
Reason for recall

A strong pull on the high-pressure transfer hose of cryosurgical unit may lead to pneumatic short circuit between he gas inlet and the connector resulting in CO2 leaking into the return path, leading to excessive pressure causing the cryoprobe to rupture.

Action

On June 26, 2026, Erbe USA issued a Urgent: Medical Device Correction update notification to affected consignees via multiple methods ( Email/Website/Hand delivery). ERBE ask consignees to take the following actions: 1. We request the ERBECRYO 2 Unit be made available to the Erbe Representative to install the (V)1.0.4 Software. The Erbe Representative will perform all tasks required to update the software. 2. Confirm acknowledgement with Erbe Representative on-site. 3. Share this notice with all users within your facility. 4.While awaiting software update, there is no change of the Cryosurgical Unit s intended use or performance. Please continue to follow all warnings, instructions, guidelines, etc. involved with the Unit and Cryoprobe.

Distribution pattern

US Nationwide distribution including in the states and territories of Alabama, Alaska, Arizona, Arkansas, California, Colorado, Connecticut, Delaware, District of Columbia, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nebraska, Nevada, New Hampshire, New Jersey, New Mexico, New York, North Carolina, North Dakota, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Vermont, Virginia, Washington, West Virginia, Wisconsin, Wyoming.

K numbers
K190651
Harmonized identifiers (openFDA)
Device name
Unit, Cryosurgical, Accessories
Medical specialty description
General, Plastic Surgery
Regulation number
878.4350
Device class
2
K number
K222356, K240776, K060859, K111859, K152668, K970995, K161615, K882568, K212814, K953637, K161337, K922878, K914591, K991122, K011073, K021261, K912529, K243245, K141110, K203024, K171626, K230599, K964047, K993965, K061510, K172041, K160273, K242932, K240106, K261806, K172373, K881349, K042667, K040809, K170810, K964971, K163244, K811390, K051509, K954703 +224 more
Registration number
1417592, 2937707, 3003678543, 3004753330, 1526711, 3039443708, 3008262715, 3012913237, 3008309062, 3013283620, 3015895145, 3011307964, 3009470597, 3026606306, 3015612252, 3013077751, 3010885402, 3008797959, 3009762450, 3015733082, 9610614, 1450662, 3004099264, 3015309643, 2134265, 3042940623, 3013445151, 3012697079, 3005740500, 3002808022, 3007829657, 9613249, 3014527929, 3008252257, 3017820152, 3012627460, 1424263, 1811755, 3015177815, 3039443404 +70 more
FEI number
1000208912, 1417592, 2937707, 3003678543, 3004753330, 1526711, 3039443708, 3008262715, 3012913237, 3008309062, 3000215205, 3013283620, 3015895145, 3011307964, 3009470597, 3026606306, 3015612252, 3013077751, 3010885402, 3008797959, 3009762450, 3015733082, 2000004234, 1450662, 3004099264, 3015309643, 3042940623, 3001236277, 1000140327, 1000122656, 3005740500, 3002808022, 3007829657, 3014527929, 3008252257, 3017820152, 3012627460, 1811755, 3015177815, 3039443404 +70 more
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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.