Buffered Lidocaine 1% with Sodium Bicarbonate Injection for Local Anesthetic Use (Concentration=10 mg/mL) 0.25 mL Total Volume, Rx only , SCA Pharmaceuticals, 8821 Knoedl Ct. Little Rock, AR 72205 877-550-5059
Reported: July 18, 2018 Initiated: June 29, 2018 #D-0918-2018
Product Description
Buffered Lidocaine 1% with Sodium Bicarbonate Injection for Local Anesthetic Use (Concentration=10 mg/mL) 0.25 mL Total Volume, Rx only , SCA Pharmaceuticals, 8821 Knoedl Ct. Little Rock, AR 72205 877-550-5059
Reason for Recall
Subpotent Drug: Stability data does not support the current expiration dating of 55 days after compounding.
Details
- Recalling Firm
- SCA Pharmaceuticals
- Units Affected
- 3984 syringes
- Distribution
- United States
- Location
- Little Rock, AR
Frequently Asked Questions
What product was recalled? ▼
Buffered Lidocaine 1% with Sodium Bicarbonate Injection for Local Anesthetic Use (Concentration=10 mg/mL) 0.25 mL Total Volume, Rx only , SCA Pharmaceuticals, 8821 Knoedl Ct. Little Rock, AR 72205 877-550-5059. Recalled by SCA Pharmaceuticals. Units affected: 3984 syringes.
Why was this product recalled? ▼
Subpotent Drug: Stability data does not support the current expiration dating of 55 days after compounding.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on July 18, 2018. Severity: Moderate. Recall number: D-0918-2018.
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