LidoPatch (lidocaine HCl 3.6%, menthol 1.25%) Pain Relief Patch, packaged in 1 patch/box (NDC 10882-527-01); 30 patches/box (NDC 10882-527-02 and 10882-527-04), Manufactured for: JAR Laboratories, Elmhurst, IL.
Reported: June 3, 2020 Initiated: May 19, 2020 #D-1277-2020
Product Description
LidoPatch (lidocaine HCl 3.6%, menthol 1.25%) Pain Relief Patch, packaged in 1 patch/box (NDC 10882-527-01); 30 patches/box (NDC 10882-527-02 and 10882-527-04), Manufactured for: JAR Laboratories, Elmhurst, IL.
Reason for Recall
CGMP Deviations: due to the loss of product manufacturing records and retain product samples, there is no assurance that the product will remain within specification through the labeled expiration date.
Details
- Recalling Firm
- Wuhan Bingbing Pharmaceutical Co., Ltd.
- Units Affected
- 4,960 boxes
- Distribution
- Nationwide in the USA
- Location
- Wuhan, N/A
Frequently Asked Questions
What product was recalled? ▼
LidoPatch (lidocaine HCl 3.6%, menthol 1.25%) Pain Relief Patch, packaged in 1 patch/box (NDC 10882-527-01); 30 patches/box (NDC 10882-527-02 and 10882-527-04), Manufactured for: JAR Laboratories, Elmhurst, IL.. Recalled by Wuhan Bingbing Pharmaceutical Co., Ltd.. Units affected: 4,960 boxes.
Why was this product recalled? ▼
CGMP Deviations: due to the loss of product manufacturing records and retain product samples, there is no assurance that the product will remain within specification through the labeled expiration date.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on June 3, 2020. Severity: Moderate. Recall number: D-1277-2020.
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