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 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
