Class II · Moderate risk Terminated
Midazolam 1 mg/mL
Reason Lack of Assurance of Sterility: Potential leakage of bags.
Is Chloride recalled?
Yes — there is an active recall. 326 ongoing FDA recalls mention Chloride (1,994 total). Check the affected lots below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Chloride. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed.
Class II · Moderate risk Terminated
MAGnesium 4gm in NS 100 mL
Reason Lack of Assurance of Sterility: Potential leakage of bags.
Class II · Moderate risk Terminated
HYDROmorphone 1 mg/mL
Reason Lack of Assurance of Sterility: Potential leakage of bags.
Class II · Moderate risk Terminated
fentaNYL
Reason Lack of Assurance of Sterility: Potential leakage of bags.
Class II · Moderate risk Terminated
EPINEPHrine
Reason Lack of Assurance of Sterility: Potential leakage of bags.
Class II · Moderate risk Terminated
ePHEDrine 50mg
Reason Lack of Assurance of Sterility: Potential leakage of bags.
Class II · Moderate risk Terminated
ceFAZolin 2 gm in NS 100mL. ceFAZolin Sodium
Reason Lack of Assurance of Sterility: Potential leakage of bags.
Class II · Moderate risk Terminated
0.2% ROPivacaine - OnQ Pump
Reason Lack of Assurance of Sterility: Potential leakage of bags.
Class II · Moderate risk Terminated
Irinotecan Hydrochloride Injection
Reason Superpotent Drug: High out of specification assay value results for potency.
Class II · Moderate risk Terminated
Irinotecan Hydrochloride Injection
Reason Superpotent Drug: High out of specification assay value results for potency.
Class II · Moderate risk Terminated
HYDROmorphone HCl 0.5 mg per mL in 0.9% Sodium Chloride
Reason Superpotent and Subpotent
Class I · High risk Terminated
Naloxone Hydrochloride Injection
Reason Presence of Particulate Matter; Potential for particulate matter on the syringe plunger.
Class II · Moderate risk Terminated
0.9% Sodium Chloride Injection
Reason Lack of assurance of sterility: Bags have potential to leak.
Class II · Moderate risk Terminated
0.9% Sodium Chloride Injection
Reason Lack of assurance of sterility: Bags have potential to leak.
Class II · Moderate risk Terminated
0.9% Sodium Chloride Injection
Reason Lack of assurance of sterility: Bags have potential to leak.
Class II · Moderate risk Terminated
0.45% Sodium Chloride Injection
Reason Lack of assurance of sterility: Bags have potential to leak.
Class III · Low risk Terminated
Riomet
Reason Labeling: Not Elsewhere Classified: Sun Pharma has decided to initiate this recall in response to identified labeling discrepancies in the patient literature.
Class III · Low risk Terminated
Diltiazem CD
Reason Failed Dissolution Specifications. High dissolution results were obtained during stability testing.
Class III · Low risk Terminated
Vasopressin 50 Units added to 250 mL 0.9% Sodium Chloride Injection USP
Reason cGMP deviations
Class II · Moderate risk Terminated
Sodium Chloride 3% Inh. 4 mL NEP #30 NDC 00487-9003-60 30 days supply.
Reason Lack of Processing Controls.
Class II · Moderate risk Terminated
WipeEssentials Wet Wipes
Reason CGMP Deviations: finished products were manufactured with poor quality water.
Class II · Moderate risk Terminated
Levetiracetam in 0.54% Sodium Chloride Injection
Reason Lack of Assurance of Sterility; confirmed customer report of a leaking bags and mold found between the outer bag and the overwrap
Class II · Moderate risk Terminated
Levetiracetam in 0.75% Sodium Chloride Injection
Reason Lack of Assurance of Sterility; confirmed customer report of a leaking bags and mold found between the outer bag and the overwrap
Class II · Moderate risk Terminated
Levetiracetam in 0.82% Sodium Chloride Injection
Reason Lack of Assurance of Sterility; confirmed customer report of a leaking bags and mold found between the outer bag and the overwrap
Class III · Low risk Terminated
Tramadol Hydrochloride 50 mg tablets
Reason Labeling: Incorrect or Missing Lot and/or Exp Date
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