Class II U.S. Food and Drug Administration

Hangzhou Bever Medical Devices Co., Ltd. BD Ready-to-Use Hydrophilic Catheter 14 Fr recall: Labeling error, Incorrect expiration date

Recall published 9 months ago

Labeling error, Incorrect expiration date

The hazard: Mislabelling or misbranding

Misbranding prompted this recall. The agency treats a label that misstates the contents as seriously as it treats contamination, because people act on labels.

What the notice says: Labeling error, Incorrect expiration date

Why it matters: The product carries the wrong label, the wrong lid or the wrong packaging. The food inside is generally fine; the problem is that the package describes something else, which defeats anyone relying on it.

Symptoms and when to call a doctor

There is no illness associated with mislabelling itself. The exception is where the undeclared contents include an allergen, in which case treat it as an allergen recall and watch for the reaction that person normally has.

This page is general information, not medical advice. If you feel unwell, a clinician who can see you is the only person able to judge your case.

Recall details

Recall number
Z-1061-2026
Published
January 21, 2026
Risk level
Class II
Status
Ongoing
Issued by
U.S. Food and Drug Administration
Brand
Hangzhou Bever Medical Devices Co., Ltd.
Product type
Medical devices
Units affected
149310 units
Distribution
Nationwide
Made in
China
Lot / code info
UDI: (01)06948796204063/Lot # T21823
UPC codes
06948796204063

Products covered by this recall

BD Ready-to-Use Hydrophilic Catheter 14 Fr (4.7 mm) Straight Tip, Coated, Female REF: RTU14F

Check your product

The notice names 3 codes you can read straight off the package. Type the one printed on yours and the list below narrows to it.

UPC / barcode

Read the twelve digits under the barcode on the package.

  • 06948796204063

Lot or batch code

Usually ink-stamped near the seam, the cap or the bottom of the pack.

  • T21823 — 149310 units

Model or item number

On the rating label, the box or the instruction sheet.

  • RTU14F — UDI

Codes are lifted verbatim from the FDA — Device enforcement notice. A code that is missing here may still be covered — the official notice is the complete list.

What to do about Mislabelled

Hangzhou Bever Medical Devices Co., Ltd. — Misbranding prompted this recall. The agency treats a label that misstates the contents as seriously as it treats contamination, because people act on labels.

  1. Read the official notice to see what is actually inside the pack, then decide whether anyone in your home needs to avoid it.
  2. Return it for a refund; a mislabelled pack is returnable whether or not it is edible for your household.
  3. Keep a photo of the mismatched label, which makes the refund conversation much shorter.
  4. Check the lot code on your pack — these mix-ups are usually confined to a short production window.

Refunds, and what else you can claim

The purchase price is the floor, not the ceiling. Where a recall caused you a real cost, say so.

  • Claim the refund at the store first; it is the fastest route and needs the least paperwork.
  • If you bought several packs over time, list them. Firms routinely settle for more than a single unit when a customer asks.
  • Medical costs, lost earnings or a spoiled event are not handled at the service desk. Write to the company contact on this page instead, with dates and documents.
  • Keep copies of everything you send. If a recall caused harm, that file is what any later claim rests on.

Company contact: HANGZHOU BEVER MEDICAL DEVICES CO., LTD. — Building 2, No. 1-1, Houmuqiao, Yongle Village, Cangqian Street, Hangzhou

The official notice

This page summarises a notice published by U.S. Food and Drug Administration. The agency notice is the authoritative version — read it before you act, and treat it as the final word if anything here looks different.

Open the FDA — Device enforcement record U.S. Food and Drug Administration recalls

Questions people ask about this recall

Why was Hangzhou Bever Medical Devices Co., Ltd. medical devices recalled?

Labeling error, Incorrect expiration date Labeling error, Incorrect expiration date

How do I know if I have the recalled product?

Match the codes printed on your package against the notice: UPC 06948796204063; lot code T21823 — 149310 units; model number RTU14F — UDI. If the code on your package is not on that list, your unit is outside the recall.

What should I do with it right now?

Read the official notice to see what is actually inside the pack, then decide whether anyone in your home needs to avoid it.

Can I get my money back?

Claim the refund at the store first; it is the fastest route and needs the least paperwork.

Where was the recalled product sold?

It was distributed nationwide.

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