Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes E P DRAPE PACK-LF DYNJ0373061J
Summary
The FDA issued a Class II for Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Sy by Medline Industries, LP. Reason: Unapproved design changes to the products outside of the 510(k) clearance..
Details
Source
Device Recall
External ID
Z-1889-2026
Action Date
2026-04-29
Status
Ongoing
Category
device
Product Description
Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes E P DRAPE PACK-LF DYNJ0373061J
Lot/Code Info: DYNJ0373061J UDI-DI 10889942396856 (EA) 40889942396857 (CS) LOT 24ABR895
Quantity Affected: 270,311 total
Reason for Recall
Unapproved design changes to the products outside of the 510(k) clearance.
Distribution
Worldwide distribution - US Nationwide and the countries of Canada, Panama, Barbados.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-02-27
Company
Northfield, IL
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 217 device recalls issued in the same week, part of 413 device-related FDA actions this month.
Medline Industries, LP has 442 FDA actions in our database, including 415 recalls and 27 clearances.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Medline Industries, LP) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Medline Industries, LP have FDA actions?
Medline Industries, LP has 442 FDA actions in our database, including 415 recalls and 27 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "Z-1889-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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