SCA Pharmaceuticals, LLC recalls Lidocaine HCl 2% 5 mL, Syringe, Rx Only, SCA Pharmaceuticals 755 Rainbow Road Windsor, CT 08695 NDC 70004-0723-09
SCA Pharmaceuticals recalls Lidocaine HCl 2% 5mL syringes due to foreign material inside vials. This may cause injury during injection. Affected products have NDC 70004-0723-09 and were sold from December 29, 2019 to January 1, 2020.
Lower-risk recall
Presence of Foreign Substance: Foreign material found inside the vial (manufacturer).
Contact the company & request your remedy
What happened, in plain English
SCA Pharmaceuticals is recalling Lidocaine HCl 2% 5 mL syringes because foreign material was found inside the vials. This could cause injury if the syringe is used for injections. Read more at govinfonow.com/recall/37669-sca-pharmaceuticals-lidocaine-2-syringe-recall-foreign-material-hazard.
Source Summary by GovInfoNow · govinfonow.com/recall/37669-sca-pharmaceuticals-lidocaine-2-syringe-recall-foreign-material-hazard · Updated October 5, 2026 · FDA enforcement record: FDA #D-0620-2020
Cite this page
“SCA Pharmaceuticals Lidocaine 2% Syringe Recall: Foreign Material Hazard.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/37669-sca-pharmaceuticals-lidocaine-2-syringe-recall-foreign-material-hazard. Based on FDA recall #D-0620-2020 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0620-2020%22&limit=1).
Why it’s dangerous
Foreign material inside the vial could cause injury during injection. The hazard is not described as causing serious injury or death in normal use.
Who’s affected
People who have the specific Lidocaine HCl 2% 5 mL syringes with NDC 70004-0723-09 are affected. Medical professionals using these syringes for injections are most at risk.
How to tell if you have this one
Check for the NDC number 70004-0723-09 on the syringe label. These products were sold between December 29, 2019 and January 1, 2020.
- Brand
SCA Pharmaceuticals- Category
Drug
What to do — step by step
Check Product Label
Look for the NDC number 70004-0723-09 on the syringe label.
Questions people ask
Is this product safe to use?
The recall states foreign material was found inside the vials, but does not specify if the product is safe to use after inspection.
What should I do if I have this product?
The recall does not provide a remedy, so no specific action is required beyond checking the label.
When was this product sold?
These products were sold from December 29, 2019 to January 1, 2020.
Contact SCA Pharmaceuticals
We’ve drafted a message you can send SCA Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0620-2020 — SCA Pharmaceuticals SCA Pharmaceuticals Hello, I own a SCA Pharmaceuticals that is covered by recall D-0620-2020 from SCA Pharmaceuticals. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-0620-2020 (November 26, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0620-2020 to see it in context.
- Plain-language summary written by qwen3:4b on October 5, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.