0.2% ROPivacaine - OnQ Pump, (ROPivacaine HCL (USP) 1100mg, 0.9% Sodium Chloride (USP) QS 550 ml, single dose pump. For: Vidant…
Reason Lack of Assurance of Sterility: Potential leakage of bags.
54 FDA recalls mention Ropivacaine. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Ropivacaine.
Reason Lack of Assurance of Sterility: Potential leakage of bags.
Reason Lack of sterility assurance.
Reason Lack of sterility assurance.
Reason Lack of sterility assurance.
Reason Lack of assurance of sterility: Three lots were released where there was a failure to follow proper testing and investigation procedures. Product may…
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 Lack of sterility assurance: Microbial growth detected during a routine simulation of the manufacturing process. No batches of distributed product…
Reason Lack of Assurance of Sterility; product has the potential to leak.
Reason Labeling: Not Elsewhere Classified: Products may contain synthetic latex and/or natural latex.
Reason Labeling: Not Elsewhere Classified: Products may contain synthetic latex and/or natural latex.
Reason Labeling: Incorrect or Missing Lot and/or Exp Date
Reason Labeling: Incorrect or Missing Lot and/or Exp Date
Reason Labeling: Incorrect or Missing Lot and/or Exp Date
Reason Labeling: Incorrect or Missing Lot and/or Exp Date
Reason Labeling: Incorrect or Missing Lot and/or Exp Date
Reason Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Reason Lack of Assurance of Sterility
Reason Lack of Assurance of Sterility
Reason Lack of Assurance of Sterility
Reason Lack of Assurance of Sterility
Reason Lack of Assurance of Sterility
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