Metoclopramide Tablets, USP 10 mg, 100-count bottle, Rx only, Manufactured in Croatia by Pliva Hrvatska, d.o.o., Zageb, Croatia…
Reason Presence of foreign tablets/capsules.
12 FDA recalls mention Metoclopramide. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Metoclopramide.
Reason Presence of foreign tablets/capsules.
Reason Lack of Assurance of Sterility
Reason Lack of Assurance of Sterility
Reason Chemical contamination; Unknown brown residue adhering to the inside of one vial.
Reason Lack of Assurance of Sterility: manufacturing areas for the recalled products exceeded acceptance levels for microbial recovery leading to a lack of…
Reason CGMP Deviations: Purified water used to manufacture the drug products may have been contaminated with Burkholderia cepacia.
Reason Defective Container: Lids on unit dose cups are not fully qualified.
Reason Defective Container: Product leaks when inverted.
Reason Presence of Particulate Matter: Potential vendor glass issue - glass spiticules (glass strands) were identified during site inspection of the vials.
Reason Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes
Reason Lack of Assurance of Sterility: Franck's Lab Inc. initiated a recall of all Sterile Human Drugs distributed between 11/21/2011 and 05/21/2012. FDA…
Reason Labeling: Correct Labeled Product Miscart/Mispack: The shipper label displayed "5 mL x 50," instead of "10 mL x 50,"
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