189 FDA recalls mention Hydromorphone. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Hydromorphone.
Reason Lack of Assurance of Sterility:Microbial contamination was detected during routine testing of subsequent unreleased product lots due to interaction…
Reason Non-Sterility: Confirmed customer complaints of glass product container vials that may be empty or cracked.
Reason Non-Sterility: Confirmed customer complaints of glass product container vials that may be empty or cracked.
Reason Lack of sterility assurance.
Reason Lack of sterility assurance.
Reason Lack of sterility assurance.
Reason Lack of sterility assurance.
Reason Lack Of Assurance Of Sterility.
Reason Lack Of Assurance Of Sterility.
Reason Superpotent drug: out of specification result for potency
Reason Lack of Assurance of Sterility.
Reason Labeling: Incorrect or Missing Lot and/or Exp. Date
Reason Lack of sterility assurance: resulting from use of a damaged sterilizing filter for nitrogen used in the manufacturing process.
Reason Lack of sterility assurance: Microbial growth detected during a routine simulation of the manufacturing process. No batches of distributed product…
Reason Presence of Particulate Matter: Silicone oil
Reason Presence of Particulate Matter: Silicone oil
Reason Presence of Particulate Matter: Silicone oil
Reason Lack of Assurance of Sterility; product has the potential to leak.
Reason Lack of assurance of sterility: Product bags leaking at seam.
Reason Labeling: Not Elsewhere Classified: Products may contain synthetic latex and/or natural latex.
Reason Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Reason Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Reason Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Reason Presence of Particulate Matter: API contaminated with glass particulate was used to produce sterile injectable drugs.
Reason Presence of Particulate Matter: API contaminated with glass particulate was used to produce sterile injectable drugs.
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