0.4 mcg/mL Sufentanil Citrate and 0.1% Bupivacaine HCl
Presence of Particulate Matter: API contaminated with glass particulate was used to produce sterile injectable drugs.
Visible foreign particles - glass, metal, fibers or other material - found in the product. Particles can enter from equipment wear, containers or the process, and are dangerous in injectables.
867 FDA drug recalls with this cause, newest first.
These recalls involve visible foreign material - glass, metal, fibers, rubber or other debris - most often found in injectable or liquid products, where nothing besides the intended ingredients should be present. It also includes foreign tablets or capsules found in a bottle of a different product. In an injectable a stray particle can go straight into the bloodstream, which is why a noticeable share of these recalls are Class I.
Presence of Particulate Matter: API contaminated with glass particulate was used to produce sterile injectable drugs.
Presence of Particulate Matter: API contaminated with glass particulate was used to produce sterile injectable drugs.
Presence of Particulate Matter: API contaminated with glass particulate was used to produce sterile injectable drugs.
Presence of Particulate Matter: API contaminated with glass particulate was used to produce sterile injectable drugs.
Presence of Particulate Matter: API contaminated with glass particulate was used to produce sterile injectable drugs.
Presence of Particulate Matter: API contaminated with glass particulate was used to produce sterile injectable drugs.
Presence of Particulate Matter: API contaminated with glass particulate was used to produce sterile injectable drugs.
Presence of Particulate Matter: API contaminated with glass particulate was used to produce sterile injectable drugs.
Presence of Particulate Matter: API contaminated with glass particulate was used to produce sterile injectable drugs.
Presence of Particulate Matter: API contaminated with glass particulate was used to produce sterile injectable drugs.
Presence of Particulate Matter: API contaminated with glass particulate was used to produce sterile injectable drugs.
Presence of Particulate Matter: Glass particulate found in sterile injectable product
Presence of Particulate Matter
Presence of Particulate Matter: Confirmed customer complaint for the presence of particulate matter.
Presence of Particulate Matter: particulate matter identified as an insect in one vial.
Presence of Particulate Matter: particulate matter identified as glass in one vial.
Presence of Foreign Substance: Product complaint for the presence of foreign matter identified as silicone within the tablet.
Presence of Particulate Matter: Glass particles found in the product after reconstitution.
Presence of Particulate Matter: Glass particles found in the product after reconstitution.
PRESENCE OF PARTICULATE MATTER: Product complaint for the presence of particulate matter identified as an insect.
Presence of Particulate Matter: identified as dried skin.
Presence of Particulate Matter: identified as a cloth fiber.
Presence of Particulate Matter: identified as cardboard.
Presence of Foreign Tablets/Capsules: Presence of a comingled Carbimazole 5 mg tablet.
Presence of Particulate Matter: Confirmed customer compliants of finding an insect floating in the primary container of each product.
Free recall alerts
Tell us what you take. When FDA posts a recall announcement or classifies a recall for one of your medications, we email you in plain English, with what to check. No account needed.