CLASS II ONGOING Drug recall · Reported 3 Jun 2020 · FDA Enforcement Report

LidoPro (lidocaine 4%, menthol recalled by Wuhan Bingbing Pharmaceutical

Wuhan Bingbing Pharmaceutical is recalling LidoPro (lidocaine 4%, menthol 5%, methyl salicylate 4%) patch, 15 Patches per, distributed nationwide in the US. The recall was initiated on 19 May 2020 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesBatch #: 170527, Exp 2020.05
Quantity recalled54,000 boxes

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-1278-2020
FDA event ID
85726
Recalling firm
Wuhan Bingbing Pharmaceutical, Wuhan, N/A
Classification
Class II
Status
Ongoing
Recall initiated
19 May 2020
FDA classified
28 May 2020
Reported
3 Jun 2020
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Drug class
Pain Medication

Timeline

19 May 2020Recall initiated by company
28 May 2020Classified by FDA+9 days
3 Jun 2020Published in enforcement report+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

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.

Product as listed by the FDA

LidoPro (lidocaine 4%, menthol 5%, methyl salicylate 4%) patch, 15 Patches per box, Manufactured For: Terrain Pharmaceuticals, Reno, NV 89501; NDC 53225-1023-1.

Where it was distributed

Nationwide in the USA

Nationwide

Questions about this recall

Why was it 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 lots are affected?

Batch #: 170527, Exp 2020.05

Where was it sold?

Nationwide in the USA

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

3 other products · FDA event 85726

More recalls from Wuhan Bingbing Pharmaceutical

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