DrugApr 13, 2016
Meditech Laboratories Formula 0 (PGE 20 mcg/mL) Injection, 5 mL vials recall — FDA D-0807-2016
Lack of Assurance of Sterility: incomplete or missing data regarding production.
Class IIFDA: TerminatedMeditech Laboratories, Inc.
Recall history in this database
Classification mix: Class II: 7.
DrugApr 13, 2016
Meditech Laboratories Formula 4 recall — FDA D-0803-2016
Lack of Assurance of Sterility: incomplete or missing data regarding production.
Class IIFDA: TerminatedMeditech Laboratories, Inc.
DrugApr 13, 2016
Meditech Laboratories Formula 9 recall — FDA D-0804-2016
Lack of Assurance of Sterility: incomplete or missing data regarding production.
Class IIFDA: TerminatedMeditech Laboratories, Inc.
DrugApr 13, 2016
Meditech Laboratories Formula 3 recall — FDA D-0806-2016
Stability Does Not Support Expiry: manufactured with an active ingredient that expired before the labeled Beyond Use Date.
Class IIFDA: TerminatedMeditech Laboratories, Inc.
DrugApr 13, 2016
Meditech Laboratories Formula 1 recall — FDA D-0805-2016
Stability Does Not Support Expiry: manufactured with an active ingredient that expired before the labeled Beyond Use Date.
Class IIFDA: TerminatedMeditech Laboratories, Inc.
DrugApr 13, 2016
Meditech Laboratories Formula 2 recall — FDA D-0802-2016
Superpotent Drug: one ingredient was found to be above assay specification.
Class IIFDA: TerminatedMeditech Laboratories, Inc.
DrugApr 13, 2016
Meditech Laboratories Formula 2 recall — FDA D-0808-2016
Stability Does Not Support Expiry: manufactured with an active ingredient that expired before the labeled Beyond Use Date.
Class IIFDA: TerminatedMeditech Laboratories, Inc.
Understanding this recall history
This page summarizes recall records in which the official source identifies Meditech Laboratories, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.