Total recalls 32 since 2019
Last 12 months 0 reported
Class I 0 0% of total
Ongoing 0 latest 1 May 2019
Recalls per month, last 24 months click a bar for that month
Severity split
Class I 0 0% Class II 32 100% Class III 0 0%
Why cmc enterprise pharmacy is recalled
All cmc enterprise pharmacy recalls, newest first 32 total
Reported Class Recall Company Reason Where 1 May 2019 Drug CLASS II Diltiazem 250 mg in NS, Made by: Enterprise Pharmacy recalled CMC Enterprise Pharmacy Sterility NC 1 May 2019 Drug CLASS II CeFAZolin 1 GM a) in NS recalled by CMC Enterprise Pharmacy CMC Enterprise Pharmacy Sterility NC 1 May 2019 Drug CLASS II Phenylephrine 20 mg NS, Made by: Enterprise Pharmacy recalled CMC Enterprise Pharmacy Sterility NC 1 May 2019 Drug CLASS II Vancomycin 1000 mg in NS, Made by: Enterprise Pharmacy recalled CMC Enterprise Pharmacy Sterility NC 1 May 2019 Drug CLASS II Vancomycin 1750 mg in 0.9% Sodium Chloride, Made recalled CMC Enterprise Pharmacy Sterility NC 1 May 2019 Drug CLASS II Magnesium Sulfate 1 GM in NS, Made by: Enterprise Pharmacy recalled CMC Enterprise Pharmacy Sterility NC 1 May 2019 Drug CLASS II Sodium Citrate 4%, 40 mg/mL syringe, Flush Syringe, Made recalled CMC Enterprise Pharmacy Sterility NC 1 May 2019 Drug CLASS II Vancomycin 1500 mg in NS, Made by: Enterprise Pharmacy recalled CMC Enterprise Pharmacy Sterility NC 1 May 2019 Drug CLASS II Norepinephrine 16 mg in NS, Made by: Enterprise Pharmacy recalled CMC Enterprise Pharmacy Sterility NC 1 May 2019 Drug CLASS II NICARdipine 25 mg in NS Excel, Made by: Enterprise Pharmacy recalled CMC Enterprise Pharmacy Sterility NC 1 May 2019 Drug CLASS II CefTRIAXone 1 GM, 100 mg/mL syringe, Made recalled CMC Enterprise Pharmacy Sterility NC 1 May 2019 Drug CLASS II Phenylephrine 0.8 mg/ NS (0.08 mg/mL), (80 mcg/mL) syringe recalled CMC Enterprise Pharmacy Sterility NC 1 May 2019 Drug CLASS II Labetalol 20 mg/, 20 mg in syringe, Made recalled CMC Enterprise Pharmacy Sterility NC 1 May 2019 Drug CLASS II Alteplase 1 mg/mL in syringe, Made by: Enterprise Pharmacy recalled CMC Enterprise Pharmacy Sterility NC 1 May 2019 Drug CLASS II Magnesium Sulfate 4 GM in NS, Made by: Enterprise Pharmacy recalled CMC Enterprise Pharmacy Sterility NC 1 May 2019 Drug CLASS II Lidocaine Buffered with J-Tip syringe, 10:1 recalled CMC Enterprise Pharmacy Sterility NC 1 May 2019 Drug CLASS II Clindamycin 900 mg in NS, Made by: Enterprise Pharmacy recalled CMC Enterprise Pharmacy Sterility NC 1 May 2019 Drug CLASS II Vancomycin 2000 mg in 0.9% Sodium Chloride, Made recalled CMC Enterprise Pharmacy Sterility NC 1 May 2019 Drug CLASS II Vancomycin 1250 mg in NS, Made by: Enterprise Pharmacy recalled CMC Enterprise Pharmacy Sterility NC 1 May 2019 Drug CLASS II Magnesium Sulfate 6 GM in NS, Made by: Enterprise Pharmacy recalled CMC Enterprise Pharmacy Sterility NC 1 May 2019 Drug CLASS II Phenylephrine 40 mg in 0.9% Sodium Chloride, 160 mcg/mL recalled CMC Enterprise Pharmacy Sterility NC 1 May 2019 Drug CLASS II Sodium Bicarbonate 150 mEq in D5W, Made recalled CMC Enterprise Pharmacy Sterility NC 1 May 2019 Drug CLASS II Heparin Pork in NS, Made by: Enterprise Pharmacy recalled CMC Enterprise Pharmacy Sterility NC 1 May 2019 Drug CLASS II Oxytocin in NS, Made by: Enterprise Pharmacy recalled CMC Enterprise Pharmacy Sterility NC 1 May 2019 Drug CLASS II Lidocaine 1% - Sodium Bicarb 8.4% 10:1 syringe recalled CMC Enterprise Pharmacy Sterility NC 1 May 2019 Drug CLASS II Lidocaine 1% - Sodium Bicarbonate 8.4% 1:1 syringe recalled CMC Enterprise Pharmacy Sterility NC 1 May 2019 Drug CLASS II DelNido Cardioplegia (Normosol-R pH 7.4 or Plasma-Lyte A pH recalled CMC Enterprise Pharmacy Sterility NC 1 May 2019 Drug CLASS II CeFAZolin 3 gm 100 mg/mL syringe, Made recalled CMC Enterprise Pharmacy Sterility NC 1 May 2019 Drug CLASS II Magnesium Sulfate 2 GM in NS, Made by: Enterprise Pharmacy recalled CMC Enterprise Pharmacy Sterility NC 1 May 2019 Drug CLASS II Dexmedetomidine 400 mcg in NS, Made by: Enterprise Pharmacy recalled CMC Enterprise Pharmacy Sterility NC
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About this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.