RecallHawk
Class II Recall

Medline Convenience kits labeled as: TONSIL & ADENOID PACK, Pack Number DYNJ43427C

MEDLINE INDUSTRIES, LP - Northfield

Summary

The FDA issued a Class II for Medline Convenience kits labeled as: TONSIL & ADENOID PACK, Pack Number DYNJ4 by MEDLINE INDUSTRIES, LP - Northfield. Reason: Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issue.

Details

Source

Device Recall

External ID

Z-3000-2024

Action Date

2024-09-18

Status

Ongoing

Category

device

Product Description

Medline Convenience kits labeled as: TONSIL & ADENOID PACK, Pack Number DYNJ43427C

Lot/Code Info: DYNJ43427C , Lot Number 21HBA933 ; DYNJ43427C , Lot Number 22ABL557 ; DYNJ43427C , Lot Number 22BBL591 ; DYNJ43427C , Lot Number 19ABE939 ; DYNJ43427C , Lot Number 19ABM274 ; DYNJ43427C , Lot Number 19ABT846 ; DYNJ43427C , Lot Number 22DBL373 ; DYNJ43427C , Lot Number 22FBV273 ; DYNJ43427C , Lot Number 22GBE783 ; DYNJ43427C , Lot Number 22HBY245 ; DYNJ43427C , Lot Number 22IBS212 ; DYNJ43427C , Lot Number 19IBD112 ; DYNJ43427C , Lot Number 22KBT930 ; DYNJ43427C , Lot Number 22KBV623 ; DYNJ43427C , Lot Number 19JBZ344 ; DYNJ43427C , Lot Number 23ABM258 ; DYNJ43427C , Lot Number 23CBQ295 ; DYNJ43427C , Lot Number 23DBQ887 ; DYNJ43427C , Lot Number 23EBQ116 ; DYNJ43427C , Lot Number 20BBH601 ; DYNJ43427C , Lot Number 23GBI661 ; DYNJ43427C , Lot Number 20DBE542 ; DYNJ43427C , Lot Number 23HBQ003 ; DYNJ43427C , Lot Number 20EBM157 ; DYNJ43427C , Lot Number 23JBX153 ; DYNJ43427C , Lot Number 20GBU737 ; DYNJ43427C , Lot Number 20HBR283 ; DYNJ43427C , Lot Number 23LBR867 ; DYNJ43427C , Lot Number 20IBB669 ; DYNJ43427C , Lot Number 20IBK144

Reason for Recall

Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.

Distribution

Worldwide distribution.

Type: Voluntary: Firm initiated

Recall Initiated: 2024-04-08

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 257 device recalls issued in the same week, part of 413 device-related FDA actions this month.

MEDLINE INDUSTRIES, LP - Northfield has 822 FDA actions in our database, including 822 recalls.

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 - Northfield) 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 - Northfield have FDA actions?

MEDLINE INDUSTRIES, LP - Northfield has 822 FDA actions in our database, including 822 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "Z-3000-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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