Reported Apr 23, 2025 · Ongoing

Medline Convenience kits used for various procedures

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 Convenience kits used for various procedures

31 of 31 products

Products covered by this recall
Model / numberProduct as published
DYNJ41097ABASIC CATARACT
DYNJ60631BPK EYE
DYNJ80316ACATARACT PACK
DYNJ63707CBASIC EYE PACK
DYNJ85284EYE PACK WITH ACCESSORY PACK
DYNJ44748IPHACO PACK
DYNJ17004LCAROMONT EYE TRAY-LF
SYNJ10271BCHOG MINOR OPHTHALMIC PACK
DYNJ80082LIFESPAN VITRECTOMY PACK
DYNJ48256MDR KEYS EYE PACK 2
DYNJ55508BVITRECTOMY PACK
DYNJ63952AEYE PACK
DYNJ67309CVITRECTOMY
DYNJ24516FCATARACT PACK-MARY IMMACUL-LF
DYNJ57258GDR FLOOD EYE PACK
DYNJ67875BLEPH PACK
DYNJ17004LCAROMONT EYE TRAY-LF
DYNJ47859CEYE PLASTIC PACK
SYNJ10259AOPHTHALMOLOGY PACK
DYNJ45667CPLASTIC EYE
Lot codes and dates

31 of 31 products

Products covered by this recall
#BarcodesProduct as published
11019348999442140193489994422Lot Number: 24IBF244; 2) DYNJ60631B, UDI-DI: 10193489994421(each), 40193489994422(case)
21019532724522140195327245222Lot Number: 24IBG352; 3) DYNJ80316A, UDI-DI: 10195327245221(each), 40195327245222(case)
31019348988350340193489883504Lot Number: 24IBG593; 4) DYNJ63707C, UDI-DI: 10193489883503(each), 40193489883504(case)
41019532748645740195327486458Lot Number: 24IBH027; 5) DYNJ85284, UDI-DI: 10195327486457(each), 40195327486458(case)
51019348927345840193489273459Lot Number: 24IBH266; 6) DYNJ44748I, UDI-DI: 10193489273458(each), 40193489273459(case)
61019348924414440193489244145Lot Number: 24IBH805; 7) DYNJ17004L, UDI-DI: 10193489244144(each), 40193489244145(case)
71019348945720940193489457200Lot Number: 24IBS294; 8) SYNJ10271B, UDI-DI: 10193489457209(each), 40193489457200(case)
81019532701200740195327012008Lot Number: 24IBS393; 9) DYNJ80082, UDI-DI: 10195327012007(each), 40195327012008(case)
91019532746617640195327466177Lot Number: 24IBS417; 10) DYNJ48256M, UDI-DI: 10195327466176(each), 40195327466177(case)
101019532726691240195327266913Lot Number: 24JBJ668; 11) DYNJ55508B, UDI-DI: 10195327266912(each), 40195327266913(case)
111019348939395840193489393959Lot Number: 24JBN908; 12) DYNJ63952A, UDI-DI: 10193489393958(each), 40193489393959(case)
121019532766899040195327668991Lot Number: 24JBT060; 13) DYNJ67309C, UDI-DI: 10195327668990(each), 40195327668991(case)
131019532727845840195327278459Lot Number: 24JBT766; 14) DYNJ24516F, UDI-DI: 10195327278458(each), 40195327278459(case)
141019532749112340195327491124Lot Number: 24JBU088; 15) DYNJ57258G, UDI-DI: 10195327491123(each), 40195327491124(case)
151019348944882540193489448826Lot Number: 24JBV026; 16) DYNJ67875, UDI-DI: 10193489448825(each), 40193489448826(case)
161019348924414440193489244145Lot Number: 24JBW137; 17) DYNJ17004L, UDI-DI: 10193489244144(each), 40193489244145(case)
171019348991606540193489916066Lot Number: 24JBX679; 18) DYNJ47859C, UDI-DI: 10193489916065(each), 40193489916066(case)
181019348978687340193489786874Lot Number: 24KBA576; 19) SYNJ10259A, UDI-DI: 10193489786873(each), 40193489786874(case)
191019348999106240193489991063Lot Number: 24KBB063; 20) DYNJ45667C, UDI-DI: 10193489991062(each), 40193489991063(case)
201019845910027740198459100278Lot Number: 24KBC142; 21) DYNJ81548B, UDI-DI: 10198459100277(each), 40198459100278(case)
Amount recalled
3909 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

There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

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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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 6:58 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.