Catheter Recall: BD Ready-to-Use Hydrophilic 14 Fr Straight Tip
Announced 2026-01-21 · FDA
Hangzhou Bever Medical Devices Co., Ltd. is recalling the BD Ready-to-Use Hydrophilic Catheter 14 Fr Straight Tip due to labeling error and an incorrect expiration date. Approximately 149,310 units were distributed in the United States, including Georgia. The recall number is UDI: (01)06948796204063/Lot # T21823.
| Brand | HANGZHOU BEVER MEDICAL DEVICES CO., LTD. |
|---|---|
| Product | BD Ready-to-Use Hydrophilic Catheter 14 Fr (4.7 mm) Straight Tip, Coated, Female REF: RTU14F |
| Reason | Labeling error, Incorrect expiration date |
| Severity | moderate |
| Units affected | 149310 |
| Distribution | US Nationwide distribution in the state of GA. |
| Agency | FDA |
WHAT YOU SHOULD DO
- Do not use the recalled device if you own one until advised otherwise.
- Check your packaging or documentation for the lot number T21823 to determine if your unit is affected.
- Contact the distributor or manufacturer for instructions on disposal, return, or replacement.
- If you experienced any problems, report them to the FDA's MedWatch program.
How to identify the recalled item
| Lot / date codes | UDI: (01)06948796204063/Lot # T21823 |
|---|---|
| Lot / date codes | UDI: (01)06948796204063/Lot # T21823 |
These are the identifiers FDA published for this recall. Most recall notices list no UPC or model number at all — if the code on your item is not shown here, that does not mean the item is excluded. Check the official notice, or contact the company.
This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.