Para-Pak Clean Vial-For the collection, transportation, preservation, and examination of stool specimens containing inte
Summary
The FDA issued a Class II for Para-Pak Clean Vial-For the collection, transportation, preservation, and examin by Meridian Bioscience Inc. Reason: Plastic vials contain a manufacturing defect may cause an increased risk of leakage and presents a risk of incidental exposure to biological hazards .
Details
Source
Device Recall
External ID
Z-0519-2024
Action Date
2023-12-20
Status
Ongoing
Category
device
Product Description
Para-Pak Clean Vial-For the collection, transportation, preservation, and examination of stool specimens containing intestinal parasites Catalog Number: 900312
Lot/Code Info: UDI-DI: 00840733101892 Lot Numbers: 509940Q Expiration Date: 09/12/2030
Quantity Affected: 571 Cases
Reason for Recall
Plastic vials contain a manufacturing defect may cause an increased risk of leakage and presents a risk of incidental exposure to biological hazards associated with direct contact with the patient specimen.
Distribution
Nationwide Foreign: Italy
Type: Voluntary: Firm initiated
Recall Initiated: 2023-10-19
Company
Cincinnati, OH
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 238 device recalls issued in the same week, part of 403 device-related FDA actions this month.
Meridian Bioscience Inc has 14 FDA actions in our database, including 9 recalls and 5 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 (Meridian Bioscience Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Meridian Bioscience Inc have FDA actions?
Meridian Bioscience Inc has 14 FDA actions in our database, including 9 recalls and 5 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "Z-0519-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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