Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
Z-1438-2024Class II

Centurion Hemostat kits labeled as: a) STERILE CURV KELLY HEMOSTAT, Product Code 65340; b) STERILE CURV...

MEDLINE INDUSTRIES, LP - Northfield / initiated 2024-02-23 / Open, Classified / root cause: manufacturing process

MEDLINE INDUSTRIES, LP - Northfield began a recall of Centurion Hemostat kits labeled as: a) STERILE CURV KELLY HEMOSTAT, Product Code 65340; b) STERILE CURV MOSQUITO HEMOSTAT (MHS103), Product Code 66145; c)... on . FDA classified it as Class II and gives the reason as "Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users". As of , the recall status on record is Open, Classified, and MDM tags the root cause as manufacturing process.

Recall record

Recall number
Z-1438-2024
Classification
Class II
Status
Open, Classified
Initiated
Posted
Recalling firm
MEDLINE INDUSTRIES, LP - Northfield
Product
Centurion Hemostat kits labeled as: a) STERILE CURV KELLY HEMOSTAT, Product Code 65340; b) STERILE CURV MOSQUITO HEMOSTAT (MHS103), Product Code 66145; c) STERILE STRT KELLY HEMOSTAT (SK8039), Product Code 66170; d) STERILE CURV KELLY HEMOSTAT (CK8040), Product Code 66175; e) STERILE CURV SATIN HEMOSTAT (MHS103S), Product Code 66445; f) STERILE STRT SATIN HEMOSTAT (MHS102S), Product Code 66485; g) STERILE STRT KELLY HEMOSTAT (SK8039S), Product Code 66695; h) STERILE STRAIGHT KELLY HEMOSTAT, Product Code 67140; i) ST. STR MOSQUITO HEMOSTAT 3 1/2"(MHB700), Product Code 67325; j) STERILE CVD MOSQT HEMOST 3 1/2"(MHB710), Product Code 67330; k) STERILE 8" CRVD KELLY HEMOSTAT (CK1008), Product Code 67655; l) STERILE 8" STR KELLY HEMOSTAT (SK1008), Product Code 67660; m) ST MOSQUITO HEMO CURVED FINE PT (P/S), Product Code I68100; n) ST CURVED KELLY HEMOSTAT-TAMPA GEN, Product Code I68310; o) STERILE STRT KELLY HEMOSTAT (ZM-09417), Product Code P-65240; p) STERILE STRT MOSQUITO HEMOSTAT (MHS102), Product Code TRI66140; q) STERILE CURVED KELLY HEMO (ST153), Product Code TRI66765
Product code
HRQ Hemostat
Reason for recall
Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
Root cause tag
manufacturing process
FDA root cause
Process control
Action
Medline Industries, LP, issued a Medical Device Recall notice to its consignees on 02/27/2024 via email and USPS First Class mail. The notice explained the problem with the devices, risk, and requested that the products be destroyed at the consignee. Distributors were directed to notify their customers.
Quantity in commerce
80903 units
Distribution
Worldwide distribution - US Nationwide and the countries of Panama, Canada.
Product codes and lots
a) 65340, UDI/DI 10653160038023 (case) 00653160038026 (each), Lot Numbers: 2023041090, 2023061290, 2023091190; b) 66145, UDI/DI 70653160008783 (case) 00653160008784 (each), Lot Numbers: 2023042690, 2023042790, 2023072790; c) 66170, UDI/DI 70653160024035 (case) 00653160024036 (each), Lot Numbers: 2023031090, 2023041790; d) 66175, UDI/DI 60653160039575 (case) 00653160039573 (each), Lot Numbers: 2023031390, 2023050990, 2023082490, 2023103090; e) 66445, UDI/DI 70653160023779 (case) 00653160023770 (each), Lot Numbers: 2023070390, 2023071090; f) 66485, UDI/DI 60653160029200 (case) 00653160029208 (each), Lot Numbers: 2023042690, 2023090790; g) 66695, UDI/DI 60653160024861 (case) 00653160024869 (each), Lot Numbers: 2023042790; h) 67140, UDI/DI 60653160049871 (case) 00653160049879 (each), Lot Numbers: 2023112990; i) 67325, UDI/DI 10653160110675 (case) 00653160110678 (each), Lot Numbers: 2023042490; j) 67330, UDI/DI 30653160110730 (case) 00653160110739 (each), Lot Numbers: 2023042890; k) 67655, UDI/DI 10653160196006 (case) 00653160196009 (each), Lot Numbers: 2023030290; l) 67660, UDI/DI 10653160196013 (case) 00653160196016 (each), Lot Numbers: 2023031390, 2023101990; m) I68100, UDI/DI 10653160235811 (case) 00653160235814 (each), Lot Numbers: 2023041190, 2023060790; n) I68310, UDI/DI 00653160278835 (case) 10653160278832 (each), Lot Numbers: 2023022190; o) P-65240, UDI/DI 10653160359234 (case) 20653160359231 (each), Lot Numbers: 2023120590; p) TRI66140, UDI/DI 00653160317855 (case) 10653160317852 (each), Lot Numbers: 2023032890, 2023061690; q) TRI66765, UDI/DI 00653160317947 (case) 10653160317944 (each), Lot Numbers: 2023030990

Enforcement reports

One row per recalled product line
FDA enforcement reports joined to recall event Z-1438-2024
Recall numberClassStatusVoluntary or mandatedReport dateClassified
Z-1427-2024Class IIOngoingVoluntary: Firm initiated
Z-1428-2024Class IIOngoingVoluntary: Firm initiated
Z-1429-2024Class IIOngoingVoluntary: Firm initiated
Z-1430-2024Class IIOngoingVoluntary: Firm initiated
Z-1431-2024Class IIOngoingVoluntary: Firm initiated
Z-1432-2024Class IIOngoingVoluntary: Firm initiated
Z-1433-2024Class IIOngoingVoluntary: Firm initiated
Z-1434-2024Class IIOngoingVoluntary: Firm initiated
Z-1435-2024Class IIOngoingVoluntary: Firm initiated
Z-1436-2024Class IIOngoingVoluntary: Firm initiated
Z-1437-2024Class IIOngoingVoluntary: Firm initiated
Z-1438-2024Class IIOngoingVoluntary: Firm initiated
Z-1439-2024Class IIOngoingVoluntary: Firm initiated
Z-1440-2024Class IIOngoingVoluntary: Firm initiated
Z-1441-2024Class IIOngoingVoluntary: Firm initiated
Z-1442-2024Class IIOngoingVoluntary: Firm initiated
Z-1443-2024Class IIOngoingVoluntary: Firm initiated
Z-1444-2024Class IIOngoingVoluntary: Firm initiated
Z-1445-2024Class IIOngoingVoluntary: Firm initiated
Z-1446-2024Class IIOngoingVoluntary: Firm initiated
Z-1447-2024Class IIOngoingVoluntary: Firm initiated
Z-1448-2024Class IIOngoingVoluntary: Firm initiated
Z-1449-2024Class IIOngoingVoluntary: Firm initiated
Z-1450-2024Class IIOngoingVoluntary: Firm initiated
Z-1451-2024Class IIOngoingVoluntary: Firm initiated
Z-1452-2024Class IIOngoingVoluntary: Firm initiated
Z-1453-2024Class IIOngoingVoluntary: Firm initiated
Z-1454-2024Class IIOngoingVoluntary: Firm initiated
Z-1455-2024Class IIOngoingVoluntary: Firm initiated