Summary
The FDA issued a Class II for HARDY DIAGNOSTICS CatScreen, 25dsk/vial by MEDLINE INDUSTRIES, LP - Northfield. Reason: Product stored incorrectly in temperature controlled setting instead of refrigeration..
Details
Source
Device Recall
External ID
Z-0554-2022
Action Date
2022-02-09
Status
Terminated
Category
device
Product Description
HARDY DIAGNOSTICS CatScreen, 25dsk/vial
Lot/Code Info: Model Number HADZ110, all lots
Quantity Affected: 100 units (4 packs, 25 per pack)
Reason for Recall
Product stored incorrectly in temperature controlled setting instead of refrigeration.
Distribution
US Nationwide distribution in the state of California.
Type: Voluntary: Firm initiated
Recall Initiated: 2021-12-01
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 95 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-0554-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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