Diazepam Injection, USP, 10 mg Automatic, Autoinjector for Buddy Use, 5 mg/mL, 2 mL recall — FDA D-1369-2012
Impurities/Degradation Products: High Out of Specification levels for carbostyril, a known degradation product of diazepam.
Browse U.S. drug recall enforcement reports from the FDA in a structured, searchable format. Review the recalled product, reason, firm, status, dates, distribution information and FDA classification when available.
10,690 detailed records are currently available in this category.
Impurities/Degradation Products: High Out of Specification levels for carbostyril, a known degradation product of diazepam.
Presence of Particulate Matter: A single visible particulate was observed in a retention sample bottles identified as stainless steel
Short Fill: These products are being recalled because there is potential that vials with low fill volume were released into distribution.
Presence of Particulate Matter: In the course of inspecting retention samples visual particles were observed.
Lack of Assurance of Sterility: Bausch & Lomb, Inc. is recalling 7 Lots of Murocel Methylcellulose Lubricant Opthalmic Solution 1% (15 mL). Product was found to be OOS for Antimicrobial…
Impurities/Degradation Products: Out Of Specification levels of nitrogen dioxide.
Miscalibrated and/or Defective Delivery System: Out of Specification results for mechanical peel force and/or the z-statistic value which relates to the patient's ability to remove the…
Miscalibrated and/or Defective Delivery System: Out of Specification results for mechanical peel force and/or the z-statistic value which relates to the patient's ability to remove the…
Short Fill: These products are being recalled because there is potential that vials with low fill volume were released into distribution.
Miscalibrated and/or Defective Delivery System: Out of Specification results for mechanical peel force and/or the z-statistic value which relates to the patient's ability to remove the…
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