Device recalls

Generic Name: Perma Sharp Sutures; Generic Name: Polypropylene Nonabsorbable Surgical Suture; Model/Catalog Number: PSN8698P (HSI Item No.…

Henry Schein Inc. · Products lack 510(k) clearance.

Open, ClassifiedProcess controlZ-0338-2027
Open FDA's page for this record
Cfres ID
223144
Product res number
Z-0338-2027
Event date initiated
2026-09-17
Event date posted
2026-11-03
Recall status
Open, Classified
Res event number
100016
Product code
GAW
Code info
Model/Catalog Number: PSN8698P (HSI Item No. 600-5659); UDI-DI: 10889950001957; Lot Number: 0624014HF;
Firm FEI number
1000143438
Recalling firm
Henry Schein Inc.
Address 1
41 Weaver Rd
City
Denver
State
PA
Postal code
17517-9308
Additional info contact
Tracey Alexander +1-631-4543003
Reason for recall
Products lack 510(k) clearance.
Root cause description
Process control
Product quantity
33
Distribution pattern
Worldwide distribution - U.S. Nationwide and the countries of Canada, Uganda, and the Cayman Islands.
Product description

Generic Name: Perma Sharp Sutures; Generic Name: Polypropylene Nonabsorbable Surgical Suture; Model/Catalog Number: PSN8698P (HSI Item No. 600-5659); Product Description: Sterile, synthetic, nonabsorbable, monofilament 5-0 blue polypropylene surgical suture, 18-inch length, with C-3 premium reverse-cutting needle. Component: N/A;

Action

On September 25, 2026, URGENT: MEDICAL DEVICE RECALL NOTIFICATION letters were sent to customers. ACTION: Please examine your inventory to determine whether you have affected product. If affected product is identified, immediately cease distribution and use, remove the product from available inventory, and follow the return instructions provided. The product must be returned within 30 days to Henry Schein s Returns Facility located at: 41 Weaver Rd, Denver, PA 17517.

Harmonized identifiers (openFDA)
Device name
Suture, Nonabsorbable, Synthetic, Polypropylene
Medical specialty description
General, Plastic Surgery
Regulation number
878.5010
Device class
2
K number
K041511, K930587, K000537, K113800, K010909, K141206, K902872, K171039, K931917, K980703, K062125, K133890, K162617, K173747, K193530, K021834, K052962, K171005, K961168, K100593, K042856, K992405, K983108, K904906, K914588, K002435, K060414, K113763, K221280, K945701, K143582, K093112, K903643, K920437, K180321, K192953, K131224, K142639, K994313, K954808 +45 more
PMA number
P890002, P820083
Registration number
3006562124, 3003910212, 3004111573, 3017102971, 3029901632, 3006425876, 3006981798, 3014772181, 2183744, 2523835, 1219930, 2648623, 3012494290, 1055236, 2648650, 1064584, 3009142291, 3013548553, 3032543753, 3014615644, 3018052045, 9710098, 2528981, 3008912461, 3004112621, 9617547, 3008483449, 1320468, 3014592276, 3020983460, 3018094310, 2030624, 1061124, 3035387162, 3004365956, 1000274611, 3045855232, 3013187142, 3013517171, 1054241 +75 more
FEI number
3006562124, 3003910212, 3004111573, 3017102971, 3029901632, 3006425876, 3002807993, 3014772181, 3006981798, 2183744, 2523835, 1219930, 2648623, 3000302153, 3003040625, 3012494290, 3003495548, 1000112877, 2648650, 3009142291, 3013548553, 3032543753, 3014615644, 3018052045, 1000512168, 2528981, 3008912461, 3004112621, 3008483449, 3018094310, 3014592276, 3020983460, 1000274611, 3035387162, 3004365956, 3045855232, 3013187142, 3013517171, 3009513193, 3025431509 +75 more
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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.