Reported Dec 11, 2024 · Ongoing
MEDLINE 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?
175 of 175 products
| Model / number | Barcodes | Product as published |
|---|---|---|
CDS820075V | 1019348984697340193489846974 | UDI/DI 10193489846973 (each) 40193489846974 (case), Lot Numbers: 22GBP851 |
CDS820075W | 1019532720979740195327209798 | UDI/DI 10195327209797 (each) 40195327209798 (case), Lot Numbers: 22HBH009, 23ABB066, 22JBX603, 22JBX483, 23ABM869, 22LBB096, 23EBB528, 23FBH057 |
CDS980774M | 1019348938371340193489383714 | UDI/DI 10193489383713 (each) 40193489383714 (case), Lot Numbers: 22JBT027, 23ABE914, 22KBE813, 23ABR052, 23GBL705, 24ABK006, 23JBQ162, 23LBT739, 23LBT825 |
CDS981322AB | 1019348992999740193489929998 | UDI/DI 10193489929997 (each) 40193489929998 (case), Lot Numbers: 22DBS923, 23EBE751, 23BBE438, 23HBS136 |
CDS981322AC | 1019532753948140195327539482 | UDI/DI 10195327539481 (each) 40195327539482 (case), Lot Numbers: 23LBJ448, 23LBJ388, 24BBF433, 24DMH817 |
CDS982398I | 1019532702944940195327029440 | UDI/DI 10195327029449 (each) 40195327029440 (case), Lot Numbers: 22HBF545, 22IBC664, 22JBL415, 22LBH995, 23BBS835, 23LBA643, 23JBV944, 23IBE632, 23HBJ717, 23EBP485, 24ABO332, 23FBS672, 24BBK936, 24EBC031, 24DBD943, 24CBU322, 24GBD705 |
CDS983450L | 1019348937233540193489372336 | UDI/DI 10193489372335 (each) 40193489372336 (case), Lot Numbers: 23ABF826, 23BBG537, 22FBS278, 22KBE444, 23JBR792 |
CDS983869J | 1019532745761740195327457618 | UDI/DI 10195327457617 (each) 40195327457618 (case), Lot Numbers: 23HDA541 |
CDS984261J | 1019532713962940195327139620 | UDI/DI 10195327139629 (each) 40195327139620 (case), Lot Numbers: 22IBF149, 23EBG169, 23CBE760, 22LBJ360, 22KBS546, 22KBS547 |
CDS984516L | 1019532733862640195327338627 | UDI/DI 10195327338626 (each) 40195327338627 (case), Lot Numbers: 23FDA887, 23HDB446, 23LDA038, 23JDB032, 23IDB803, 24ADA525, 23LDB093 |
CDS984516M | 1019532762984740195327629848 | UDI/DI 10195327629847 (each) 40195327629848 (case), Lot Numbers: 24BDB731, 24BDA997 |
CDS984902K | 1019532715692340195327156924 | UDI/DI 10195327156923 (each) 40195327156924 (case), Lot Numbers: 22LBH577, 23KBB878, 23HBU537, 23ABM570, 24ABI595, 24ABD063 |
CDS984902L | 1019532758495540195327584956 | UDI/DI 10195327584955 (each) 40195327584956 (case), Lot Numbers: 24DBI303 |
CDS985282F | 1019348964560640193489645607 | UDI/DI 10193489645606 (each) 40193489645607 (case), Lot Numbers: 22GBE278, 22FBL413, 22JBU598, 23DBL267, 23CBR985, 23BBN513, 23BBN776, 22KBR845, 23FBD738 |
CDS985326G | 1019532709117040195327091171 | UDI/DI 10195327091170 (each) 40195327091171 (case), Lot Numbers: 22GBJ024, 22GBF342, 22GBT686, 22FBR937, 23DBB697, 23ABJ487, 23JBU241 |
CDS985505G | 1019532741255540195327412556 | UDI/DI 10195327412555 (each) 40195327412556 (case), Lot Numbers: 23HBK247, 23GBD611, 23JBN811, 23JBN997 |
CDSCCR611Q | 1019532739866840195327398669 | UDI/DI 10195327398668 (each) 40195327398669 (case), Lot Numbers: 23GBU646, 23IBG367, 23KBJ756, 23JBS637 |
DYNJ0100978K | 1019532733900540195327339006 | UDI/DI 10195327339005 (each) 40195327339006 (case), Lot Numbers: 23GDB484, 23DDA636 |
DYNJ0101147G | 1019532705988040195327059881 | UDI/DI 10195327059880 (each) 40195327059881 (case), Lot Numbers: 22JMF390, 22LMD489, 23BMA081, 23GMI901, 23HMH876, 23JMI277, 23JMH328 |
DYNJ0101562I | 1019348996193540193489961936 | UDI/DI 10193489961935 (each) 40193489961936 (case), Lot Numbers: 22GDA866, 22FDA774 |
- Amount recalled
- 58765 units
This recall covers 28 products
The agency filed one notice per product. You are reading one of them; the other 27 are below.
15 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
Medline is recalling medical convenience manufactured using certain lots of SafeAir Smoke Evacuation Pencil which were subsequently recalled by Stryker.
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.
Free recall alerts
Get alerted about new MEDLINE INDUSTRIES, LP - Northfield recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.