Metoclopramide Injection USP, 10 mg/2 mL (5 mg/mL), 25x2mL Single Dose Vials, Rx only, Distributed by Teva Pharmaceuticals, USA, Inc., Parsippany, NJ Vial NDC 0703-4502-01 (vial) NDC# 0703-4502-04 (tray)
Reported: March 10, 2021 Initiated: February 15, 2021 #D-0297-2021
Product Description
Metoclopramide Injection USP, 10 mg/2 mL (5 mg/mL), 25x2mL Single Dose Vials, Rx only, Distributed by Teva Pharmaceuticals, USA, Inc., Parsippany, NJ Vial NDC 0703-4502-01 (vial) NDC# 0703-4502-04 (tray)
Reason for Recall
Chemical contamination; Unknown brown residue adhering to the inside of one vial.
Details
- Recalling Firm
- Teva Pharmaceuticals USA
- Units Affected
- 9,452 cartons
- Distribution
- Nationwide, including Puerto Rico
- Location
- Parsippany, NJ
Frequently Asked Questions
What product was recalled? ▼
Metoclopramide Injection USP, 10 mg/2 mL (5 mg/mL), 25x2mL Single Dose Vials, Rx only, Distributed by Teva Pharmaceuticals, USA, Inc., Parsippany, NJ Vial NDC 0703-4502-01 (vial) NDC# 0703-4502-04 (tray). Recalled by Teva Pharmaceuticals USA. Units affected: 9,452 cartons.
Why was this product recalled? ▼
Chemical contamination; Unknown brown residue adhering to the inside of one vial.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on March 10, 2021. Severity: Moderate. Recall number: D-0297-2021.
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