CritiCore Automated Urine Output and Temperature Monitor
FDA Recall Z-2243-2018 · Posted None
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Recalling FirmC.R. Bard, Inc.
Recall StatusOpen, Classified
Product CodeEXS
Date Initiated2017-11-10
Reason for Recall
Issues identified with the monitor including urine output measurement errors, temperature measurement errors and undesired alarms.
Firm Action
On Nov 10, 2017 Bard Medical sent notification letter to all their consignees informing them of the following:
Action required:
"Immediately examine your inventory and quarantine product subject to this recall. Please refer to CritiCore MonitorAffected Serial Numbers (Attachment 2) to help you locate the affected product serial number. Do not use or furtherdistribute any affected product.
"Please complete and return the accompanying Recall & Effectiveness Check Form (Attachment 1) attached to thisletter regardless of whether you have any of the affected product. Additional instructions for product return arecontained on the form.
"If you have further distributed any units with the referenced serial numbers, please identify your customers and notifythem at once of this product recall: Your notification should include a copy of this letter and the accompanying enclosures.
Please complete this form by 11/24/2017 and fax to 1-770-784-6469 or email a scanned copy to [email protected] . If you have affected product, please contact the BMD Customer Service via phone at 1-800-526-4455 option 5 and again option 5 or email [email protected] to obtain a Return Goods Authorization number (RGA #). Fax this form to 1-770-784-6469 or email a scanned copy to [email protected]. Attn: Recall Coordinator
This recall should be carried out to the user level.
Root Cause
Other
Distribution Pattern
AR, AZ, CA, FL, GA, HI, IN, JP, KS, LA, MD, MN, MO, MS, NC, NJ, OH, OK, TN, TX, VA, WA, WI, and WY
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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