Vicryl Plus Sutures: Vicryl Plus Suture 18"(45cm) 3-0 recall
VICRYL PLUS Sutures: VICRYL PLUS SUTURE 18"(45CM) 3-0 VIO VICRYL PLUS SUTURE 18"(45CM) 0 UND VICRYL PLUS SUTURE 18"(45CM) 0 VIO VICRYL PLUS SUTURE…
Why was Vicryl Plus Sutures: Vicryl Plus Suture 18"(45cm) 3-0 recalled?
VICRYL Suture, VICRYL Plus Suture, PDS Suture- may contain product that does not match the sales unit carton and foil label.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Product Name/Product Code/Lot Numbers: VICRYL PLUS SUTURE 18"(45CM) 3-0 VIO VCP713D MJ6586 VICRYL PLUS SUTURE 18"(45CM) 4-0 UND VCP714D MJZ386 VICRYL PLUS SUTURE 18"(45CM) 0 UND VCP724D MJM852 VICRYL PLUS SUTURE 18"(45CM) 0 VIO VCP727D MH2267 VICRYL PLUS SUTURE 18"(45CM) 3-0 VIO VCP738D MJ7656 VICRYL PLUS SUTURE 18"(45CM) 0 VIO VCP740D MH2821 VICRYL PLUS SUTURE 18"(45CM) 1 VIO VCP753D MGM113 VICRYL PLUS SUTURE 18"(45CM) 2-0 UND VCP762D MGK480 MK5042 MKK981 VICRYL PLUS SUTURE 18"(45CM) 4-0 VIO VCP773D MGZ815 VICRYL PLUS SUTURE 18"(45CM) 2-0 VIO VCP775D ML2512 VICRYL PLUS SUTURE 27"(70CM) 3-0 VIO VCP784D MJM663 VICRYL PLUS SUTURE 27"(70CM) 2-0 VIO VCP785D MK6998 VICRYL PLUS SUTURE 18"(45CM) 2-0 UND VCP839D ME2930 MK2929 ML7047 VICRYL PLUS SUTURE 18"(45CM) 1 UND VCP841D MG2339 VICRYL PLUS SUTURE 18"(45CM) 3-0 UND VCP864D MK2923 VICRYL PLUS SUTURE 27"(70CM) 0 UND VCPP41D MK6415 ML5418 VICRYL PLUS SUTURE 27"(70CM) 2-0 UND VCPP42D MG6757
- Product
- VICRYL PLUS Sutures: VICRYL PLUS SUTURE 18"(45CM) 3-0 VIO VICRYL PLUS SUTURE 18"(45CM) 0 UND VICRYL PLUS SUTURE 18"(45CM) 0 VIO VICRYL PLUS SUTURE…
- Recalling firm
- Ethicon, Inc.
- Quantity
- 550,681 eaches (WW) Total
- Distribution
- Worldwide distributions - US Nationwide and countries of AUSTRALIA BELGIUM CANADA CHINA ISRAEL JAPAN PUERTO RICO SINGAPORE
- Recall date
- April 24, 2019
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)