Reported Oct 30, 2024 · Ongoing
Medline brand medical procedure convenience kits, labeled as
MEDLINE INDUSTRIES, LP - Northfield
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: MEDLINE INDUSTRIES, LP - Northfield · 3 Lakes Dr · Northfield, IL · 60093-2753
Is this the product you have?
Medline brand medical procedure convenience kits, labeled as
13 of 13 products
| Model / number | Product as published |
|---|---|
DYNJ42735A | PLASTIC PACK |
DYNJ43457 | DR SELEM PACK |
DYNJ46717A | BREAST PK TEGH-LF |
DYNJ46717A | BREAST PK TEGH-LF |
DYNJ53205B | BREAST BIOPSY-LF |
DYNJ53205B | BREAST BIOPSY-LF |
DYNJ57895 | PLASTIC PACK |
DYNJ62803 | SEPTOPLASTY PACK WRO-LF |
DYNJ64376 | BREAST PACK |
DYNJ66619A | CSTM PK SURGISTART MAINE PLAST |
DYNJ68030 | PLASTIC PACK |
DYNJ68062 | CUSTOM PLASTIC PACK |
DYNJ84997 | PLASTIC LIMB SJHC-LF |
- Lot codes and dates
13 of 13 products
Products covered by this recall # Barcodes Product as published 1 4088827722643310888277226432DYNJ42735A, UDI/DI 40888277226433 (each), 10888277226432 (case), Lot Numbers: 23LBP975 2 4088827705530910888277055308DYNJ43457, UDI/DI 40888277055309 (each), 10888277055308 (case), Lot Numbers: 23LBS052 3 4019348965001410193489650013DYNJ46717A, UDI/DI 40193489650014 (each), 10193489650013 (case), Lot Numbers: 24ABF270 4 4019348965001410193489650013DYNJ46717A, UDI/DI 40193489650014 (each), 10193489650013 (case), Lot Numbers: 23LBO013 5 4019348942485110193489424850DYNJ53205B, UDI/DI 40193489424851 (each), 10193489424850 (case), Lot Numbers: 24ABC805 6 4019348942485110193489424850DYNJ53205B, UDI/DI 40193489424851 (each), 10193489424850 (case), Lot Numbers: 23LBN742 7 4088994279037210889942790371DYNJ57895, UDI/DI 40889942790372 (each), 10889942790371 (case), Lot Numbers: 23KBF265 8 4019348968899410193489688993DYNJ62803, UDI/DI 40193489688994 (each), 10193489688993 (case), Lot Numbers: 23LBN303 9 4019348980784510193489807844DYNJ64376, UDI/DI 40193489807845 (each), 10193489807844 (case), Lot Numbers: 24ABD094 10 4019532742784010195327427849DYNJ66619A, UDI/DI 40195327427840 (each), 10195327427849 (case), Lot Numbers: 23LBU414 11 4019348946928910193489469288DYNJ68030, UDI/DI 40193489469289 (each), 10193489469288 (case), Lot Numbers: 23LBL117 12 4019348947458010193489474589DYNJ68062, UDI/DI 40193489474580 (each), 10193489474589 (case), Lot Numbers: 24ABC304 13 4019532744421210195327444211DYNJ84997, UDI/DI 40195327444212 (each), 10195327444211 (case), Lot Numbers: 23LBK468 - Amount recalled
- 1048 units
This recall covers 34 products
The agency filed one notice per product. You are reading one of them; the other 33 are below.
21 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the pouch is opened/unsealed.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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