Lidocaine HCl 2% 5 mL, Syringe, Rx Only, SCA Pharmaceuticals 755 Rainbow Road Windsor, CT 08695 ...

FDA Drug Recall #D-0620-2020 — Class II — November 26, 2019

Recall Summary

Recall Number D-0620-2020
Classification Class II — Moderate risk
Date Initiated November 26, 2019
Status Terminated
Voluntary Voluntary: Firm initiated

Recalling Firm

Firm SCA Pharmaceuticals, LLC
Location Windsor, CT
Product Type Drugs
Quantity 1363 syringes

Product Description

Lidocaine HCl 2% 5 mL, Syringe, Rx Only, SCA Pharmaceuticals 755 Rainbow Road Windsor, CT 08695 NDC 70004-0723-09

Reason for Recall

Presence of Foreign Substance: Foreign material found inside the vial (manufacturer).

Distribution Pattern

nationwide

Lot / Code Information

1219012595 29-Dec-19 1219012647 01-Jan-20

Other Recalls from SCA Pharmaceuticals, LLC

Recall # Classification Product Date
D-0417-2024 Class II PHENYLephrine HCl 5000 mcg/50 mL in 0.9% Sodium... Nov 9, 2023
D-0411-2024 Class II labetalol HCl 20 mg/4mL Injection, (Concentrati... Nov 9, 2023
D-0410-2024 Class II HYDROmorphone HCl 30 mg/30 mL in 0.9% Sodium Ch... Nov 9, 2023
D-0419-2024 Class II PHENYLephrine HCl 40 mg in 0.9% Sodium Chloride... Nov 9, 2023
D-0399-2024 Class II fentaNYL 100 mcg/50 mL, Bupivacaine HCl 0.125% ... Nov 9, 2023

Frequently Asked Questions

Stop taking the medication and contact your pharmacist or doctor immediately. For Class I recalls, this is urgent. For Class II or III recalls, consult your doctor before stopping — abruptly discontinuing certain medications (blood pressure drugs, antidepressants, diabetes medications) can be more harmful than continuing while arranging a replacement. Check whether the recall applies to your specific lot number and expiration date. Return the product to your pharmacy and report any adverse effects to FDA MedWatch at 1-800-FDA-1088.

Not necessarily. Many drug recalls are initiated because of quality system failures or test results that suggest a product might not meet specifications — even if no patients have reported harm. The FDA uses a precautionary approach: if there is reason to believe quality standards were not met, a recall is required regardless of whether adverse effects have been reported. Class I recalls typically involve a reasonable probability of harm; Class II recalls may cause temporary health issues; Class III recalls are for products unlikely to cause adverse health consequences but that still violate regulations.

Pharmacies typically receive recall notices directly from drug wholesalers and manufacturers within days of the recall being announced. Your pharmacist can look up whether any product in your prescription history matches a recalled lot number. For current recalls, the FDA publishes updates at FDA.gov/safety/recalls-market-withdrawals-safety-alerts and sends MedWatch email alerts for significant drug safety issues. You can sign up for MedWatch alerts at FDA.gov. Most major pharmacy chains also have their own recall notification systems that automatically alert pharmacists when a recalled product is in their inventory.

What Should You Do?

Stop using this medication if affected by this recall. Contact your pharmacist or prescribing doctor immediately for guidance. Do not flush medications — use a drug take-back program.