SODIUM CHLORIDE 0.9% Sodium Chloride Injection, USP, 250 mL VIAFLEX Plastic Container Bag recall — FDA D-0957-2016
Presence of Particulate Matter: Confirmed customer compliants of finding an insect floating in the primary container of each product.
Overview of recall records associated with Baxter Healthcare Corp., including dates, categories and classifications where available.
Classification mix: Class I: 9, Class II: 2.
Presence of Particulate Matter: Confirmed customer compliants of finding an insect floating in the primary container of each product.
Presence of Particulate Matter: Confirmed customer compliants of finding an insect floating in the primary container of each product.
Lack of Assurance of Sterility: potential for leaking containers which lacks the assurance of sterility.
Presence of Particulate Matter: identified as dried skin.
Presence of Particulate Matter: Customer complaint for an insect found free floating inside a single bag for each lot recalled.
Presence of Particulate Matter: Customer complaint for an insect found free floating inside a single bag for each lot recalled.
Presence of Particulate Matter and Lack of Assurance of Sterility: The firm received a complaint for customer of presence of particulate matter, leaky containers, and missing port…
Presence of Particulate Matter: Products recalled due to presence of particulate matter (metal)
Presence of Particulate Matter: Products recalled due to presence of particulate matter (metal)
Presence of Particulate Matter: Products recalled due to presence of particulate matter (metal)
Presence of Particulate Matter: Products recalled due to presence of particulate matter (metal)
This page summarizes recall records in which the official source identifies Baxter Healthcare Corp. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.