succinylcholine 200 mg/10 mL (20 mg/mL), Syringe, Rx only, this drug was repackaged by CAPS Inc, 2200 South 43rd Avenue Pheonix, AZ, NDC 72196-6011-2.
Reported: August 9, 2023 Initiated: July 14, 2023 #D-0949-2023
Product Description
succinylcholine 200 mg/10 mL (20 mg/mL), Syringe, Rx only, this drug was repackaged by CAPS Inc, 2200 South 43rd Avenue Pheonix, AZ, NDC 72196-6011-2.
Reason for Recall
Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Details
- Recalling Firm
- Central Admixture Pharmacy Services, Inc.
- Units Affected
- 26,208 Syringes
- Distribution
- Nationwide in the USA
- Location
- Phoenix, AZ
Frequently Asked Questions
What product was recalled? ▼
succinylcholine 200 mg/10 mL (20 mg/mL), Syringe, Rx only, this drug was repackaged by CAPS Inc, 2200 South 43rd Avenue Pheonix, AZ, NDC 72196-6011-2.. Recalled by Central Admixture Pharmacy Services, Inc.. Units affected: 26,208 Syringes.
Why was this product recalled? ▼
Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on August 9, 2023. Severity: Moderate. Recall number: D-0949-2023.
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