Teva Pharmaceuticals USA recalls Lidocaine Patch 5% (700 mg) ,(NDC 0591-3525-11), 30 envelopes containing 1 patch each/ 30 Patches/Carton (NDC
Teva Pharmaceuticals USA recalls Lidocaine 5% patches (NDC 0591-3525-11) due to failed stability specifications. Consumers should check product lot numbers and contact Teva for details.
Lower-risk recall
Failed Stability Specifications
Contact the company & request your remedy
What happened, in plain English
Teva Pharmaceuticals USA is recalling Lidocaine 5% patches (700 mg) because they failed stability tests. This means the patches may not work properly over time, potentially causing ineffective pain relief. Read more at govinfonow.com/recall/40582-teva-lidocaine-patches-5-recall-failed-stability-specifications.
Source Summary by GovInfoNow · govinfonow.com/recall/40582-teva-lidocaine-patches-5-recall-failed-stability-specifications · Updated October 7, 2026 · FDA enforcement record: FDA #D-0857-2018
Cite this page
“Teva Lidocaine Patches 5% Recall: Failed Stability Specifications.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/40582-teva-lidocaine-patches-5-recall-failed-stability-specifications. Based on FDA recall #D-0857-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0857-2018%22&limit=1).
Why it’s dangerous
The patches failed stability specifications, meaning they may not maintain their intended effectiveness over time. This could lead to the patches not working properly when needed for pain relief.
Who’s affected
People who own or use Lidocaine 5% patches with lot numbers 1147020B (carton) or 1147020 (patch) are affected. Those using the patches for pain relief are most at risk of ineffective treatment.
How to tell if you have this one
Check the carton lot number (1147020B) and patch lot number (1147020) on the product packaging. The product is sold in 30-patch envelopes with NDC 0591-3525-11.
- Brand
Teva Pharmaceuticals USA- Category
Drug
What to do — step by step
Check Product Lot Numbers
Look for carton lot number 1147020B and patch lot number 1147020 on the packaging.
Questions people ask
Why is this patch being recalled?
The patches failed stability specifications, meaning they may not work properly over time.
How do I know if I have the recalled product?
Check the carton lot number (1147020B) and patch lot number (1147020) on the packaging.
What should I do with the recalled patches?
The recall record does not specify a remedy, so contact Teva Pharmaceuticals USA for further instructions.
Contact Teva Pharmaceuticals USA
We’ve drafted a message you can send Teva Pharmaceuticals USA to request your refund or repair — edit it as you like.
Subject: Recall D-0857-2018 — Teva Pharmaceuticals USA Teva Pharmaceuticals USA Hello, I own a Teva Pharmaceuticals USA that is covered by recall D-0857-2018 from Teva Pharmaceuticals USA. 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-0857-2018 (April 30, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0857-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 7, 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.