Device recalls

Cascade IOMAX Cortical Module, REF: 190296-200

Cadwell Industries Inc · There is the potential that an electroneurodiagnostic medical device insulator may be installed incorrectly which could result in arcing to patient connections…

Open, ClassifiedProcess designZ-1882-2024
Open FDA's page for this record
Cfres ID
207342
Product res number
Z-1882-2024
Event date initiated
2024-04-23
Event date posted
2024-05-22
Recall status
Open, Classified
Res event number
94504
Product code
GWF
Product description
Cascade IOMAX Cortical Module, REF: 190296-200
Firm FEI number
3020018
Recalling firm
Cadwell Industries Inc
Address 1
909 N Kellogg St
City
Kennewick
State
WA
Postal code
99336-7669
Additional info contact
Jason Ford 509-735-6481
Root cause description
Process design
Product quantity
54 units
Code info

UDI-DI: 00840067100653/ Serial numbers: 19029603AA1223002 19029603AA1223003 19029603AA1223004 19029603AA1223005 19029603AA1223006 19029603AA1223007 19029603AA1223011 19029603AA1223012 19029603AA1223013 19029603AA1223014 19029603AA1223015 19029603AA1223016 19029603AA1223017 19029603AA1223018 19029603AA1223019 19029603AA1223020 19029603AA1223024 19029603AB1223021 19029603AB1223023 19029603AA1223025 19029603AA0124001 19029603AA0124002 19029603AA0224008 19029603AA0124007 19029603AA0124012 19029603AA0124017 19029603AA0124004 19029603AA0124010 19029603AA0124016 19029603AA0224010 19029603AA0124015 19029603AA1223026 19029603AA0124008 19029603AA0124009 19029603AA1223027 19029603AA1223028 19029603AA1223029 19029603AA0124003 19029603AA0224001 19029603AA1223030 19029603AA1223008 19029603AA1223009 19029603AA0124013 19029603AA1223031 19029603AA1223001 19029603AA0224002 19029603AA0224003 19029603AA0224004 19029603AA0224005 19029603AA0224006 19029603AA0224007 19029603AA0124014 19029603AA0224009 19029603AA0124011

Reason for recall

There is the potential that an electroneurodiagnostic medical device insulator may be installed incorrectly which could result in arcing to patient connections resulting in potential unintended shock to the patient.

Action

On 4/22/24, Cadwell Industries, Inc. issued a "Urgent: Medical Device Recall" notification to affected consignees via Email: 1. Cease use of the device immediately and return all identified devices to Cadwell Industries, Inc. 2. Please complete the attached response form and return via email to quality@cadwell.com. 3. Please circulate this notice to all those who require awareness within your organization or to any organization whom you may have transferred the IOMAX Cortical Module to. 4. Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA s MedWatch Adverse Event Reporting program either online, by regular mail or by fax.

Distribution pattern

Worldwide - US Nationwide distribution in the state of MD and the countries of Mexico, Canada, Malaysia, India, Taiwan, Saudi Arabia, European Union, Switzerland, South Africa, Iraq, United Kingdom.

K numbers
K162199
Harmonized identifiers (openFDA)
Device name
Stimulator, Electrical, Evoked Response
Medical specialty description
Neurology
Regulation number
882.1870
Device class
2
K number
K162873, K912775, K863175, K130403, K162199, K870567, K931923, K780539, K080499, K112052, K020400, K071969, K844707, K962458, K971740, K971819, K051357, K851300, K142624, K944547, K010087, K093304, K915652, K912685, K822744, K872106, K991899, K111647, K160280, K822214, K820908, K002773, K091457, K962457, K110140, K040358, K844992, K965065, K212166, K060847 +101 more
Registration number
8030229, 3016438694, 3024996452, 3010123206, 8021774, 2027467, 3013501110, 9611896, 1030489, 3003851073, 1526534, 3011790297, 3017636737, 3001687738, 3010611950, 3016852448, 3018094310, 3007770159, 1319639, 3010047454, 1221763, 3004753785, 3009973505, 1119189, 2133772, 3030412764, 9612501, 2184161, 9615126, 3014251656, 1047843, 3009973336, 2024311, 3023852420, 9612330, 3006418479, 3010041499, 8043933, 3010209365, 3005545216 +48 more
FEI number
1000113738, 3016438694, 3024996452, 3010123206, 2027467, 3002957361, 3013501110, 3002809369, 3003851073, 1000116116, 1526534, 3008647423, 1000139867, 3003495548, 3011790297, 3017636737, 3001687738, 3002980729, 3001610756, 3010611950, 3016852448, 3001236549, 3018094310, 3002808356, 3007770159, 3002716534, 3010047454, 1221763, 3004753785, 3009973505, 1119189, 1000132370, 3030412764, 1000138054, 3002619595, 3003058448, 3014251656, 1047843, 3009973336, 2024311 +48 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.