FDA Recall
Terminated
Historical recordClass II
Epinephrine, ABJT 0.1 mg/mL, 10 mL, 20GX1.5 (10 pack), Rx only, MFG: Pfizer, NDC 04094-933-01
by Mckesson Medical-Surgical Inc. Corporate Office
- Reason
- cGMP deviations: Temperature abuse
- Published
- June 15, 2022
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Depo-Medrol (methylprednisolone acetate injectable suspension, USP) 80mg/mL, packaged in a) 1 mL single-dose vial (NDC# 0009-3475-01), b) 25-count box (NDC 0009-3475-03), Rx only, MFG: Pfizer
by Mckesson Medical-Surgical Inc. Corporate Office
- Reason
- cGMP deviations: Temperature abuse
- Published
- June 15, 2022
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Depo-Medrol (methylprednisolone acetate injectable suspension, USP) 40 mg/mL, 1 mL single-dose vial, Rx only, MFG: Pfizer, NDC 0009-3073-03
by Mckesson Medical-Surgical Inc. Corporate Office
- Reason
- cGMP deviations: Temperature abuse
- Published
- June 15, 2022
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Bupivacaine Hydrochloride, USP 0.5% (5mg/mL), 25 vials x 50 mL per box, Rx only, MFG: Pfizer, NDC 0409-1163-01
by Mckesson Medical-Surgical Inc. Corporate Office
- Reason
- cGMP deviations: Temperature abuse
- Published
- June 15, 2022
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Labetalol Hydrochloride Tablets, USP, 100 mg, 100-count bottle, Rx only, MFG: Par Pharma, NDC 49884-122-01
by Mckesson Medical-Surgical Inc. Corporate Office
- Reason
- cGMP deviations: Temperature abuse
- Published
- June 15, 2022
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Prazosin Hydrochloride Capsules, USP, 1 mg, 100-count bottle, Rx only, MFG: Mylan Pharma, NDC 0378-1101-01
by Mckesson Medical-Surgical Inc. Corporate Office
- Reason
- cGMP deviations: Temperature abuse
- Published
- June 15, 2022
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Loperamide Hydrochloride capsules, USP, 2 mg, 100-count bottle, Rx only, MFG: Mylan Pharma, NDC 0378-2100-01
by Mckesson Medical-Surgical Inc. Corporate Office
- Reason
- cGMP deviations: Temperature abuse
- Published
- June 15, 2022
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Duraclon (clonidine HCl injection, USP), 1000 mcg/10 mL (100 mcg/mL), 10 mL single-dose vial, Rx only, MFG: Mylan Pharma, NDC 67457-218-10
by Mckesson Medical-Surgical Inc. Corporate Office
- Reason
- cGMP deviations: Temperature abuse
- Published
- June 15, 2022
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Proventil HFA, (Albuterol Sulfate Inhalation Aerosol), 200 metered inhalations, Rx only, MFG: Merck Company, NDC 0085-1132-04
by Mckesson Medical-Surgical Inc. Corporate Office
- Reason
- cGMP deviations: Temperature abuse
- Published
- June 15, 2022
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Celestone Soluspan (betamethasone sodium phosphate and betametasone acetate injectable suspension 6 mg/mL, 30 mg/5mL, multidose vial, Rx only, MFG: Merck Company, NDC 0085-4320-01
by Mckesson Medical-Surgical Inc. Corporate Office
- Reason
- cGMP deviations: Temperature abuse
- Published
- June 15, 2022
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Levofloxacin Tablets, 500 mg, 100-count unit dose box, Rx only, MFG: Major Pharma, NDC 0904-6352-61
by Mckesson Medical-Surgical Inc. Corporate Office
- Reason
- cGMP deviations: Temperature abuse
- Published
- June 15, 2022
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Kinevac (Sincalide for Injection), 5mcg per vial, 10 vials per box, Rx only, MFG: Bracco Diagnostics Inc., NDC 0270-0556-15
by Mckesson Medical-Surgical Inc. Corporate Office
- Reason
- cGMP deviations: Temperature abuse
- Published
- June 15, 2022
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Gastrografin (Diatrizoate Meglumine and Diatrizoate Sodium Solution USP), packaged in: Twenty-four 30 mL single dose bottles, Rx only, MFG: Bracco Diagnostics Inc., NDC 0270-0445-35
by Mckesson Medical-Surgical Inc. Corporate Office
- Reason
- cGMP deviations: Temperature abuse
- Published
- June 15, 2022
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
E-Z-Gas II, Effervescent Granules, Net Weight: 4 g, 50 packets per box, MFG: Bracco Diagnostics Inc., NDC 0270-9020-01 (discontinued), NDC 10361-793-01 (current)
by Mckesson Medical-Surgical Inc. Corporate Office
- Reason
- cGMP deviations: Temperature abuse
- Published
- June 15, 2022
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
E-Z-HD (Barium Sulfate for Oral Suspension), 98% w/w, 340 g bottle, Rx only, MFG: Bracco Diagnostics Inc., NDC 32909-764-01
by Mckesson Medical-Surgical Inc. Corporate Office
- Reason
- cGMP deviations: Temperature abuse
- Published
- June 15, 2022
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Transderm Scop (scopolamine) Transdermanl System, 1 mg/ 3 days, 10 (patches) transdermal Systems Multipack, Rx only, MFG: Baxter Healthcare Corp, NDC 10019-553-03
by Mckesson Medical-Surgical Inc. Corporate Office
- Reason
- cGMP deviations: Temperature abuse
- Published
- June 15, 2022
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Recothrom Thrombin Topical (Recombinant), 5,000 units, packaged in a box containing a 5000-unit vial of RECOTHROM with a 5-mL prefilled diluent syringe (containing sterile 0.9% sodium chloride, USP), a sterile needle-free transfer device, a 5-mL sterile empty syringe, and a pre-printed label, Rx only, MFG: Baxter, NDC# 0338-0322-01
by Mckesson Medical-Surgical Inc. Corporate Office
- Reason
- cGMP deviations: Temperature abuse
- Published
- June 15, 2022
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Revonto (dantrolene sodium for injection), 20 mg/vial, 6-count box, Rx only, MFG: US WorldMeds, Inc., NDC 78670-003-67
by Mckesson Medical-Surgical Inc. Corporate Office
- Reason
- cGMP deviations: Temperature abuse
- Published
- June 15, 2022
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Revonto (dantrolene sodium for injection), 20 mg/vial, 6-count box, Rx only, MFG: US WorldMeds, Inc., NDC 27505-003-67
by Mckesson Medical-Surgical Inc. Corporate Office
- Reason
- cGMP deviations: Temperature abuse
- Published
- June 15, 2022
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Vecuronium Bromide for Injection, 10 mg (1mg/ mL) vial, 10-count box, Rx only, MFG: Teva Pharma USA, NDC 0703-2914-03
by Mckesson Medical-Surgical Inc. Corporate Office
- Reason
- cGMP deviations: Temperature abuse
- Published
- June 15, 2022
- Distribution
- Nationwide
View recall →
Recall records are summarized from official FDA and USDA sources. Notices may be updated, reclassified, terminated, or withdrawn. Always review the linked official notice for the most current instructions.
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