Phenylephrine HCL in 0.9% Sodium Chloride 10 mL, 1 mg/10 mL (100 mcg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Company 7321 Cantrell Rd. Little Rock, AR 72207 877-666-5222, NDC 52533-171-12
Reported: August 16, 2017 Initiated: July 14, 2017 #D-1074-2017
Product Description
Phenylephrine HCL in 0.9% Sodium Chloride 10 mL, 1 mg/10 mL (100 mcg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Company 7321 Cantrell Rd. Little Rock, AR 72207 877-666-5222, NDC 52533-171-12
Reason for Recall
Lack of Sterility Assurance.
Details
- Recalling Firm
- Cantrell Drug Company
- Units Affected
- 46078 syringes
- Distribution
- Nationwide within the US
- Location
- Little Rock, AR
Frequently Asked Questions
What product was recalled? ▼
Phenylephrine HCL in 0.9% Sodium Chloride 10 mL, 1 mg/10 mL (100 mcg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Company 7321 Cantrell Rd. Little Rock, AR 72207 877-666-5222, NDC 52533-171-12. Recalled by Cantrell Drug Company. Units affected: 46078 syringes.
Why was this product recalled? ▼
Lack of Sterility Assurance.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on August 16, 2017. Severity: Moderate. Recall number: D-1074-2017.
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