Premier Toxins A & B, Diagnostic Test Kits, Catalog No. 6... (Meridian Bioscience Inc) – the kits were packaged with incorrect... (2003)
Incorrect pipettes may cause minor diagnostic test kit packaging issues.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Premier Toxins A & B, Diagnostic Test Kits, Catalog No. 616096.
Brand
Meridian Bioscience Inc
Lot Codes / Batch Numbers
Lots 616096.095, -096, and -097. Expiration Date: 23 Jul 03.
Products Sold
Lots 616096.095, -096, and -097. Expiration Date: 23 Jul 03.
Meridian Bioscience Inc is recalling Premier Toxins A & B, Diagnostic Test Kits, Catalog No. 616096. due to The kits were packaged with incorrect dispensing pipettes.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The kits were packaged with incorrect dispensing pipettes.
Recommended Action
Per FDA guidance
The firm notified their affected consignees by letter on 9/23/2003.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026