FDAClass IIJuly 8, 2026

Medline Convenience Kits: 1) LUMBAR PUNCTURE CHOICE recall

Medline Convenience Kits: 1) LUMBAR PUNCTURE CHOICE, Model Number: DYNDH1215

Why was Medline Convenience Kits: 1) LUMBAR PUNCTURE CHOICE recalled?

The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

1) DYNDH1215, UDI-DI: 10889942550876(each), 40889942550877(case), Lot Number: 2025092390

Product
Medline Convenience Kits: 1) LUMBAR PUNCTURE CHOICE, Model Number: DYNDH1215
Recalling firm
Medline Industries, LP
Quantity
420 kits
Distribution
US Nationwide distribution.
Recall date
July 8, 2026
Classification
Class II
Status
Ongoing
Agency
FDA (device)
Open FDA enforcement record Latest recalls