Torrance, Co Has Recalled Injection Drugs

[Wendy]

(SafetyAlerts) - The Food and Drug Administration (FDA) released the following information.

PRODUCT
a) HYDROCHLORIC ACID Injection, 2 mg/mL (1:500), Sterile, 100 mL
Multiple Dose Vial, FOR INTRAVENOUS USE, Caution: For Office,
Clinic, or Hospital Use, Innovative Professional Services,
Portage, MI. Recall # D-287-3;
b) PYRIDOXINE Injection, (Pyridoxine HCL) 100 mg/mL, Sterile, 30 ml
Multiple Dose Vial, FOR I.M. or I.V. Use, Caution: For Office,
Clinic, or Hospital Use, Innovative Professional Services,
Portage, MI. Recall # D-288-3;
c) DEXPANTHENOL Injection, (DL-Panthenol) 250 mg/mL, Sterile,
30 mL Multiple Dose Vial, FOR I.M. or I.V. Use, Caution: For
Office, Clinic, or Hospital Use, Innovative Professional Services,
Portage, MI. Recall # D-289-3;
d) FOLIC ACID Injection, (Folic acid 10mg, sodium chloride 5.5mg,
methylparaben 1.8mg, propylparaben 0.2mg), 10mg/mL, 10mL multiple
dose vial, Innovative Professional Services, Portage, MI.
Recall # D-290-3;
d) THIAMINE Injection, (Thiamine HCL 100 mg, Chlorobutenol 3mg),
100 mg/mL, Sterile, 30 mL, Multiple Dose Vial FOR I.M. or I.V.
Use, Caution: For Office, Clinic, or Hospital Use. Innovative
Professional Services, Portage, MI. Recall # D-291-3;
e) B-COMPLEX 100 Injection, (Thiamine HCl 100mg, Riboflavin 5mg,
Pyridoxine HCl 100mg, Dexpanthenol 100mg), Sterile, 30 mL Multiple
Dose Vial, FOR I.M. or SLOW I.V. USE, Caution: For Office, Clinic,
or Hospital Use, Innovative Professional Services, Portage, MI.
Recall # D-292-3;
f) EDETATE DISODIUM Injection (E.D.T.A.) 150 mg/mL, Sterile, 100 mL
Multiple Dose Vial, FOR INTRAVENOUS USE ONLY, For Office, Clinic,
or Hospital Use, Innovative Professional Services, Portage, MI.
Recall # D-293-3;
g) HYDROXO B-12 Injection, (Hydroxocobalamin 1000mcg, Sod. Chloride
8mg, Sod. Acetate, 0.33mg), 1000mcg/mL, Sterile, 30 mL Multiple
Dose Vial, FOR I.M. or S.C. USE, For Office, Clinic, or Hospital
Use, Innovative Professional Services, Portage, MI.
Recall # D-294-3.

CODE
All lots.

RECALLING FIRM/MANUFACTURER
Torrance, Co., Portage, MI, by letter dated June 26, 2003. Firm initiated recall is ongoing.

REASON
Lack of assurance of sterility by manufacturer (IPS).

VOLUME OF PRODUCT IN COMMERCE
Unknown.

DISTRIBUTION
Nationwide.