Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
Z-2570-2024Class II

Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd...

Merit Medical Systems, Inc. / initiated 2024-06-11 / Open, Classified

Merit Medical Systems, Inc. began a recall of Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: ReSolve (Catheter and Tip Suction kit), REF... on . FDA classified it as Class II and gives the reason as "Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health". As of , the recall status on record is Open, Classified.

Recall record

Recall number
Z-2570-2024
Classification
Class II
Status
Open, Classified
Initiated
Posted
Recalling firm
Merit Medical Systems, Inc.
Product
Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: ReSolve (Catheter and Tip Suction kit), REF: RTT14038MB/A The ReSolve Thoracostomy Tray is indicated for the percutaneous removal of air and fluid from the pleural space.
Product code
JOL Catheter And Tip, Suction
Reason for recall
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.
FDA root cause
No Marketing Application
Action
On 06/11/2024, the firm sent an "URGENT MEDICAL DEVICE RECALL NOTICE" Letter to customers informing them that specific Merit Medical convenience kits contain plastic syringes manufactured by Jiangsu Shenli Medical Production Co. Ltd. These syringes lack the appropriate/sufficient FDA market authorization. In addition, Merit Medical posted the Urgent Medical Device Recall letter and complete list of affected products/kits on their website at https://www.merit.com/products/documents/product-notices/. Customer are instructed to: 1. Immediately determine if any of the products identified in the attached Customer Response Form (CRF) are within their facility, quarantine them, and discontinue use and distribution. 2. Ensure that appropriate personnel within their organization are made aware of this field action. 3. If the product has been further distributed to other facilities, institutions, or manufacturers, ensure this notice is immediately shared with them. Additional distribution details may be required by health authorities. 4. Follow the attached instructions for placing the recall labels on the products containing Jiangsu Shenli syringes, which inform the users to not use the affected syringes. If additional recall labels are needed, contact Customer Service at (801) 208-4381. Product may be returned to inventory once properly over-labeled. 5.At the point of use, the Jiangsu Shenli syringes are to be discarded. Photographs of Jiangsu Shenli syringes are enclosed to assist in identification. 6.Post this URGENT MEDICAL DEVICE RECALL NOTICE and Jiangsu Shenli Syringe photographs on or near the affected products. 7.If replacement syringes are needed, contact Customer Service at (801) 208-4381 for recommended syringe suppliers. For questions contact Merit Sales Representative or Merit Customer Service at 801-208-4381, Hours: 6 am to 6 pm MST Mon.-Fri.
Quantity in commerce
7442 kits
Distribution
U.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY.
Product codes and lots
Catalog Number/UDI-DI code/Lot Numbers: RTT14038MB/A 00884450680100 T2882458 T2775532 T2692992 T2745797 T2823440 T2758669 T2882467 T2855297 T2692990 T2864420 T2762237 T2701080 T2748465 T2872143 T2853478 T2865442 T2560919 T2607047 T2617261 T2933737 T2657108 T2886240

Enforcement reports

One row per recalled product line
FDA enforcement reports joined to recall event Z-2570-2024
Recall numberClassStatusVoluntary or mandatedReport dateClassified
Z-2557-2024Class IIOngoingVoluntary: Firm initiated
Z-2558-2024Class IIOngoingVoluntary: Firm initiated
Z-2559-2024Class IIOngoingVoluntary: Firm initiated
Z-2560-2024Class IIOngoingVoluntary: Firm initiated
Z-2561-2024Class IIOngoingVoluntary: Firm initiated
Z-2562-2024Class IIOngoingVoluntary: Firm initiated
Z-2563-2024Class IIOngoingVoluntary: Firm initiated
Z-2564-2024Class IIOngoingVoluntary: Firm initiated
Z-2565-2024Class IIOngoingVoluntary: Firm initiated
Z-2566-2024Class IIOngoingVoluntary: Firm initiated
Z-2567-2024Class IIOngoingVoluntary: Firm initiated
Z-2568-2024Class IIOngoingVoluntary: Firm initiated
Z-2569-2024Class IIOngoingVoluntary: Firm initiated
Z-2570-2024Class IIOngoingVoluntary: Firm initiated
Z-2571-2024Class IIOngoingVoluntary: Firm initiated
Z-2572-2024Class IIOngoingVoluntary: Firm initiated
Z-2573-2024Class IIOngoingVoluntary: Firm initiated
Z-2574-2024Class IIOngoingVoluntary: Firm initiated
Z-2575-2024Class IIOngoingVoluntary: Firm initiated
Z-2576-2024Class IIOngoingVoluntary: Firm initiated
Z-2577-2024Class IIOngoingVoluntary: Firm initiated
Z-2578-2024Class IIOngoingVoluntary: Firm initiated
Z-2579-2024Class IIOngoingVoluntary: Firm initiated