Is Morphine recalled?
Yes — there is an active recall. 6 ongoing FDA recalls mention Morphine (190 total). Check the affected lots below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Morphine. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed.
Class II · Moderate risk Terminated Apr 11, 2018
Reason Lack of Assurance of Sterility:Microbial contamination was detected during routine testing of subsequent unreleased product lots due to interaction…
Class II · Moderate risk Terminated Mar 5, 2018
Reason Microbial Contamination of Non-Sterile Products: Bioburden out of specification results for Morphine Sulfate API.
Class II · Moderate risk Terminated Dec 27, 2017
Reason Lack of sterility assurance.
Class II · Moderate risk Terminated Dec 27, 2017
Reason Lack of sterility assurance.
Class II · Moderate risk Terminated Nov 30, 2017
Reason Lack of sterility assurance.
Class II · Moderate risk Terminated Oct 19, 2017
Reason Lack Of Assurance Of Sterility.
Class III · Low risk Terminated Sep 26, 2017
Reason Labeling: Incorrect or Missing Lot and/or Exp. Date
Class III · Low risk Terminated Sep 26, 2017
Reason Labeling: Incorrect or Missing Lot and/or Exp. Date
Class II · Moderate risk Terminated Aug 10, 2017
Reason Lack of sterility assurance: Microbial growth detected during a routine simulation of the manufacturing process. No batches of distributed product…
Class II · Moderate risk Terminated Jul 14, 2017
Reason Lack of Assurance of Sterility: Product made with recalled 0.9% sodium chloride bags which have the potential to leak.
Class II · Moderate risk Terminated Jun 15, 2017
Reason Defective container: Oral solution leaking from container.
Class II · Moderate risk Terminated May 18, 2017
Reason Lack of assurance of sterility: Product bags leaking at seam.
Class II · Moderate risk Terminated May 18, 2017
Reason Lack of assurance of sterility: Product bags leaking at seam.
Class II · Moderate risk Terminated Feb 22, 2017
Reason Labeling: Not Elsewhere Classified: Products may contain synthetic latex and/or natural latex.
Class II · Moderate risk Terminated Nov 18, 2016
Reason Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Class II · Moderate risk Terminated Jul 26, 2016
Reason Lack of Assurance of Sterility
Class II · Moderate risk Terminated Jul 26, 2016
Reason Lack of Assurance of Sterility
Class II · Moderate risk Terminated May 5, 2016
Reason Presence of Particulate Matter: API contaminated with glass particulate was used to produce sterile injectable drugs.
Class II · Moderate risk Terminated May 5, 2016
Reason Presence of Particulate Matter: API contaminated with glass particulate was used to produce sterile injectable drugs.
Class II · Moderate risk Terminated Apr 20, 2016
Reason Lack of Assurance of Sterility
Class II · Moderate risk Terminated Apr 20, 2016
Reason Lack of Assurance of Sterility
Class II · Moderate risk Terminated Apr 20, 2016
Reason Lack of Assurance of Sterility
Class II · Moderate risk Terminated Apr 20, 2016
Reason Lack of Assurance of Sterility
Class II · Moderate risk Terminated Apr 20, 2016
Reason Lack of Assurance of Sterility
Class II · Moderate risk Terminated Apr 20, 2016
Reason Lack of Assurance of Sterility