Home / Recalls / Hospira Inc. / D-0862-2017

D-0862-2017 Class I Ongoing

Recalled by Hospira Inc. — Lake Forest, IL

Recall Details

Product Type
Drugs
Report Date
May 31, 2017
Initiation Date
April 21, 2017
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
71,550 syringes

Product Description

Infant 25% DEXTROSE Injection, USP, 2.5 g (250 mg/mL), 10 mL Unit of Use Single-dose Syringe per carton, Rx only, Hospira Inc., Lake Forest, IL 60045, NDC 0409-1775-10

Reason for Recall

Presence of Particulate Matter: human hair found within an internal sample syringe.

Distribution Pattern

Nationwide in the USA and Puerto Rico

Code Information

Lot 58382EV*, Exp 1OCT 2017, *lot may be followed by 01 or 02

Other recalls by Hospira Inc.

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  • 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)
  • D-1033-2016 Class II — Vancomycin Hydrochloride for Injection, USP, 10 g, 100 mL vial, Rx only, Hospira (May 6, 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)