ETHICON, INC. recalls MONOCRYL" (poliglecaprone 25) Suture REF Y936H MONOCRYL"
See all recalls from ETHICON, INC. →Recalled Product
MONOCRYL" (poliglecaprone 25) Suture REF Y936H MONOCRYL" Sutures are indicated for use in general soft tissue approximation and/or ligation, but not for use in cardiovascular and neurological tissues, microsurgery or ophthalmic surgery.
Hazard / Issue
Due a component mix-up in manufacturing, the affected products may contain incorrect needle type/size and suture length.
Issued by
FDA
Affected States: AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, 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, WY
Lot/Code Info: Product Number: Y936H UDI-DI code: 10705031059917 Lot Number: TMMDQD
✅ What Should You Do?
- 1Contact your healthcare provider immediately to discuss this recall.
- 2Stop using the device if it is safe to do so, and contact your provider.
- 3Follow the manufacturer's remedy instructions provided in the recall notice.
- 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.
Looking for a safe alternative?
Search Amazon for MONOCRYL" (poliglecaprone 25) Suture →If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.
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