Home / Recalls / Hospira Inc. / D-1033-2016

D-1033-2016 Class II Terminated

Recalled by Hospira Inc. — Lake Forest, IL

FDA drug recall D-1033-2016 was initiated by Hospira Inc. on May 6, 2016 and is designated Class II. Reason for recall: Presence of Particulate Matter: Cardboard The recall status is terminated (terminated September 24, 2018).

Recall Details

Product Type: Drugs
Report Date: June 22, 2016
Initiation Date: May 6, 2016
Termination Date: September 24, 2018
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity

Product Description

Vancomycin Hydrochloride for Injection, USP, 10 g, 100 mL vial, Rx only, Hospira, Lake Forest, IL, NDC 0409-6510-01

Reason for Recall

Presence of Particulate Matter: Cardboard

Distribution Pattern

Nationwide

Code Information

Lot #:565003A, Exp.01 Aug 2017

Other recalls by Hospira Inc.

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D-0153-2017 Class II — Fentanyl Citrate Injection, USP, 100 mcg Fentanyl/ 2mL, Single Dose, 50 mcg/mL, (November 1, 2016)
D-1500-2016 Class II — DOBUTamine Injection, USP 250 mg/20 mL, 20 mL Vial, For IV Use Only, Must be Dil (August 15, 2016)
D-0169-2017 Class III — 5% Lidocaine HCL and 7.5% Dextrose Injection, USP, 2 mL Single-dose ampule, 5 co (June 29, 2016)
D-1359-2016 Class II — Diazepam Injection USP 10mg/2mL (5 mg/mL, 2 mL), Rx only, Hospira Inc. Lake For (June 23, 2016)
Z-1833-2016 Class II — The Plum A+ is a dual-line volumetric infusion system designed to meet the growi (March 25, 2016)
Z-1832-2016 Class II — The Plum 360 is a large volume infuser capable of delivering fluids for a variet (March 25, 2016)
D-1137-2016 Class I — Magnesium Sulfate Inj., USP 50%, 10 g/20 mL (0.5 g/mL), (4 mEq Magnesium/mL, 20 (March 23, 2016)
D-0854-2016 Class III — Magnesium Sulfate Inj., USP 50%, 10 g/20 mL (0.5 g/mL), (4 mEq Magnesium/mL, 20 (March 23, 2016)
D-0865-2016 Class I — 8.4% Sodium Bicarbonate Injection, USP 50mEq (1mEq/mL), 4.2 grams (84 mg/mL), 50 (March 18, 2016)