COBRA-OS, custom Sheath Introducer Kit, 4 French, REF: E01P2, Sterile EO, Single Use, RX Only, 5 Units
FDA Recall Z-1578-2023 · Posted 2023-05-10
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Recalling FirmMerit Medical Systems, Inc.
Recall StatusOpen, Classified
Product CodeDYB
Date Initiated2023-03-21
Product Quantity1186 units
Reason for Recall
Custom sheath Introducer contains incorrect needle size
Firm Action
On March 21, 2023 MeritMedical issued a "Urgent Medical Device Recall Notice" to affected consignees via E-Mail. In addition to informing them about the recall, MeritMedical asked consignees to take the following actions:
1. Please immediately determine if any of the devices identified in the attached Customer Response Form (CRF) are within your facility, quarantine them, and discontinue use and distribution.
2. Ensure that applicable personnel within your organization are made aware of this field action.
3. If the product has been further distributed to other facilities, institutions, or manufacturers, please ensure this notice is immediately shared with them and note the quantity distributed on the CRF. Additional distribution details may be required by health authorities.
4. Please fill out, scan and email the completed Customer Response Form to Customer Service at [email protected] within seven (7) calendar days. All affected product shipped to you must be accounted for on the CRF.
5. Please immediately return all affected lots in your possession to Merit, per the instructions in the attached CRF.
6. If you have any questions concerning this communication, please don t hesitate to contact your Merit OEM Sales Representative or Merit OEM Customer Service at (800)-637-4839| Hours: 8 am to 5 pm MST | Mon-Fri.
Root Cause
Unknown/Undetermined by firm
Distribution Pattern
US Distribution to state of: Minnesota
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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