Device recalls

Merit Medical , REF: R2275, EsophyX Z+ with SerosaFuse Implantable Fasteners, (1) Fastener Delivery Device, (2) 7.5mm Cartridges, STERILEEO…

Merit Medical Systems, Inc. · Update to IFU to provide additional information related to risk with device over-rotation and multiple deployment of fasteners.

Open, ClassifiedUnder Investigation by firmZ-1641-2025
Open FDA's page for this record
Cfres ID
213146
Product res number
Z-1641-2025
Event date initiated
2025-03-14
Event date posted
2025-04-21
Recall status
Open, Classified
Res event number
96482
Product code
ODE
Product description
Merit Medical , REF: R2275, EsophyX Z+ with SerosaFuse Implantable Fasteners, (1) Fastener Delivery Device, (2) 7.5mm Cartridges, STERILEEO,RxOnly
Code info
All Lots/ UDI: 00810275014011
Firm FEI number
1721504
Recalling firm
Merit Medical Systems, Inc.
Address 1
1600 W Merit Pkwy
City
South Jordan
State
UT
Postal code
84095-2416
Additional info contact
Merit Customer Service 801-253-1600
Reason for recall
Update to IFU to provide additional information related to risk with device over-rotation and multiple deployment of fasteners.
Root cause description
Under Investigation by firm
Product quantity
7453 units
Action

On March 14, 2025, Merit Medical issued a "Urgent Medical Device Recall Notice via E-Mail, followed by mail to affected consignees. Merit asked consignees to take the following actions: 1. Read and understand this communication and the updated IFU referenced in the attached poster. 2. There is no need to return product to Merit. 3. Post the attached poster on or near the affected products so users are aware of the updated IFU. 4. Discard the current IFU with the product at point of use. 5. Ensure that applicable personnel within your organization are made aware of this communication. 6. If the product has been further distributed to other facilities, institutions, or manufacturers, please ensure this notice is immediately shared with them. 7. If you require paper IFUs, please contact RESPONSE@merit.com. 8. Please acknowledging you are aware of the information communicated and have completed the actions required of you. 9. If you require additional product training regarding the IFU updates, please contact your Merit Sales Representative to schedule.

Distribution pattern

Worldwide - US Nationwide distribution including in the states of AL, AR, AZ, CA, CO, CT, DC, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, WA, WI, WV and the countries of Brazil, Egypt, Israel, Saudi Arabia, Spain, Thailand, Turkey, United Arab Emirates.

K numbers
K240879
Harmonized identifiers (openFDA)
Device name
Endoscopic Suture/Plication System, Gastroesophageal Reflux Disease (Gerd)
Medical specialty description
Gastroenterology, Urology
Regulation number
876.1500
Device class
2
K number
K151001, K071553, K031262, K092400, K072125, K032820, K132151, K160960, K171307, K071651, K994290, K143634, K142113, K003956, K172811, K143645, K240879, K023234, K233240, K120299
Registration number
1724474, 3015225571, 3032855354, 3006950086, 3009039068, 3033589330, 1721504, 3012536737, 3015309643, 1721676, 3033508651
FEI number
3015225571, 3032855354, 3006950086, 3009039068, 3033589330, 1721504, 3012536737, 3015309643, 1721676, 3033508651, 3003094851
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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.