Class II U.S. Food and Drug Administration

Bd Switzerland Sarl BD PhaSeal Injector Luer , REF: 515001 BD PhaSeal Injector Luer recall: Closed system drug transfer devices were shipped to the U.S. market without

Recall published 1+ years ago

Closed system drug transfer devices were shipped to the U.S. market without a U.S. version of the instructions for use, which could be an issue if a healthcare professional is prompted to review it.

The hazard: Device safety concern

This is a device enforcement record. Check whether the remedy is a correction, a software update or a removal before changing anything.

What the notice says: Closed system drug transfer devices were shipped to the U.S. market without a U.S. version of the instructions for use, which could be an issue if a healthcare professional is prompted to review it.

Why it matters: The FDA recorded an enforcement action against this device. Most device recalls are corrections rather than removals, so the device often stays in use while the manufacturer issues a fix.

Recall details

Recall number
Z-2453-2025
Published
September 3, 2025
Risk level
Class II
Status
Ongoing
Issued by
U.S. Food and Drug Administration
Brand
Bd Switzerland Sarl
Product type
Medical devices
Units affected
3,884,670
Distribution
Nationwide
Made in
Switzerland
Lot / code info
REF/UDI-DI/Lot(Expiration): 515001/00382905150012. 515003/00382905150036/2402001(31-Jul-26), 2403002(31-Aug-26), 2403003(31-Aug-26), 2404006(30-Sep-26), 2405007(31-Oct-26), 2405014(31-Oct-26), 2408005(31-Jan-27), 2408006(31-Jan-27), 2409005(28-Feb-27), 2403713(31-Aug-26), 2404001(30-Sep-26), 2404002(30-Sep-26), 2404003(30-Sep-26), 2404004(30-Sep-26), 2404005(30-Sep-26), 2410001(31-Mar-27), 2410002(31-Mar-27), 2411001(30-Apr-27), 2411002(30-Apr-27), 2411003(30-Apr-27), 2411709(30-Apr-27), 2412002(31-May-27), 2501001(30-Jun-27), 2501002(30-Jun-27), 2501003(30-Jun-27), 2502001(31-Jul-27), 2502002(31-Jul-27), 2405004(31-Oct-26), 2405008(31-Oct-26), 2407001(31-Dec-26), 2412001(31-May-27), 2503001(31-Aug-27), 2503002(31-Aug-27), 2503003(31-Aug-27), 2504001(30-Sep-27), 2504002(30-Sep-27), 2504003(30-Sep-27); 515004/00382905150043/2405001(31-Oct-26), 2408018(31-Jan-27), 2411708(30-Apr-27), 2411727(30-Apr-27); 515005/00382905150050/2403006(31-Aug-26), 2404008(30-Sep-26), 2404009(30-Sep-26), 2404010(30-Sep-26), 2404011(30-Sep-26), 2404012(30-Sep-26), 2405002(31-Oct-26), 2407010(31-Dec-26), 2409011(28-Feb-27), 2409012(28-Feb-27), 2409016(28-Feb-27), 2410007(31-Mar-27), 2410008(31-Mar-27), 2410010(31-Mar-27), 2411725(30-Apr-27), 2405003(31-Oct-26), 2407011(31-Dec-26), 2407012(31-Dec-26), 2408008(31-Jan-27), 2408009(31-Jan-27), 2409007(28-Feb-27), 2409008(28-Feb-27), 2409009(28-Feb-27), 2409010(28-Feb-27), 2501006(30-Jun-27), 2503738(31-Aug-27), 2504004(30-Sep-27); 515100/00382905151002/2504117(31-Mar-30), 2404103(31-Mar-29), 2404122(31-Mar-29), 2404123(31-Mar-29), 2406112(31-May-29), 2406113(31-May-29), 2404124(31-Mar-29), 2405130(30-Apr-29), 2407112(30-Jun-29), 2409113(31-Aug-29), 2410113(30-Sep-29), 2410114(30-Sep-29), 2411115(31-Oct-29), 2412109(30-Nov-29), 2502116(31-Jan-30), 2503112(28-Feb-30); 515102/00382905151026/2403101(28-Feb-29), 2403102(28-Feb-29), 2403103(28-Feb-29), 2403104(28-Feb-29), 2403141(28-Feb-29), 2403707(28-Feb-29), 2404130(31-Mar-29), 2404131(31-Mar-29), 2404132(31-Mar-29), 2404141(31-Mar-29), 2404143(31-Mar-29), 2409601(31-Aug-29), 2403140(28-Feb-29), 2404125(31-Mar-29), 2404126(31-Mar-29), 2404127(31-Mar-29), 2404128(31-Mar-29), 2404129(31-Mar-29), 2404142(31-Mar-29), 2409108(31-Aug-29), 2409109(31-Aug-29), 2410701(30-Sep-29), 2412108(30-Nov-29), 2412114(30-Nov-29), 2501101(31-Dec-29), 2501102(31-Dec-29), 2501103(31-Dec-29), 2501104(31-Dec-29), 2501105(31-Dec-29), 2504108(31-Mar-30), 2504109(31-Mar-30), 2504119(31-Mar-30. 515103/00382905151033/2404133(31-Mar-29), 2404134(31-Mar-29), 2404140(31-Mar-29), 2410101(30-Sep-29), 2410102(30-Sep-29), 2410103(30-Sep-29), 2410104(30-Sep-29), 2504111(31-Mar-30). 515104/00382905151040/2410119(30-Sep-29), 2410107(30-Sep-29). 515105/00382905151057/2402112(31-Jan-29), 2403122(28-Feb-29), 2403123(28-Feb-29), 2403124(28-Feb-29), 2403125(28-Feb-29), 2403127(28-Feb-29), 2404113(31-Mar-29), 2404115(31-Mar-29), 2404117(31-Mar-29), 2405101(30-Apr-29), 2405102(30-Apr-29), 2405106(30-Apr-29), 2405107(30-Apr-29), 2405108(30-Apr-29), 2405152(30-Apr-29), 2406104(31-May-29), 2406105(31-May-29), 2406106(31-May-29), 2406107(31-May-29), 2406109(31-May-29), 2407103(30-Jun-29), 2407104(30-Jun-29), 2407106(30-Jun-29), 2407107(30-Jun-29), 2407108(30-Jun-29), 2407109(30-Jun-29), 2409103(31-Aug-29), 2409602(31-Aug-29), 2411123(31-Oct-29), 2411125(31-Oct-29), 2411126(31-Oct-29), 2411707(31-Oct-29), 2412105(30-Nov-29), 2403126(28-Feb-29), 2404102(31-Mar-29), 2404110(31-Mar-29), 2404111(31-Mar-29), 2404112(31-Mar-29), 2404114(31-Mar-29), 2404116(31-Mar-29), 2404118(31-Mar-29), 2404119(31-Mar-29), 2405103(30-Apr-29), 2405104(30-Apr-29), 2405105(30-Apr-29), 2407102(30-Jun-29), 2407105(30-Jun-29), 2409104(31-Aug-29), 2409105(31-Aug-29), 2411113(31-Oct-29), 2411124(31-Oct-29), 2501112(31-Dec-29), 2501113(31-Dec-29), 2501114(31-Dec-29), 2501115(31-Dec-29), 2502106(31-Jan-30), 2502107(31-Jan-30), 2501111(31-Dec-29), 2502108(31-Jan-30), 2502109(31-Jan-30), 2502110(31-Jan-30), 2502111(31-Jan-30), 2502112(31-Ja…
UPC codes
00382905150036, 00382905150043, 00382905150050, 00382905151002, 00382905151026, 00382905151033, 00382905151040, 00382905151057

Products covered by this recall

BD PhaSeal Injector Luer (N30C), REF: 515001 BD PhaSeal Injector Luer Lock (N35), REF: 515003 BD PhaSeal Injector Luer Lock (N35C), REF: 515004 BD PhaSeal Injector Lu63er Lock (N35C Multi), REF: 515005 BD PhaSeal Protector (P14), REF: 515100 BD PhaSeal Protector (P21), REF: 515102 BD PhaSeal Protector (P21 Multi), REF: 515103 BD PhaSeal Protector (P28), REF: 515104 BD PhaSeal Protector (P50), REF: 515105 BD PhaSeal Protector (P50 Multi), REF: 515106 BD PhaSeal Protector (P53), REF: 515107 BD PhaSeal Protector (P55), REF: 515117 BD PhaSeal Connector Luer Lock (C35), REF: 515200 BD PhaSeal Connector Luer Lock (C45), REF: 515202 BD PhaSeal Y-site Connector (C80), REF: 515304 BD PhaSeal L Connector (C90), REF: 515305 BD PhaSeal Infusion Adapter (C100), REF: 515306 BD PhaSeal Infusion Adapter (C100 Multi), REF: 515307 BD PhaSeal Cap for Injector (M50), REF: 515404 BD PhaSeal Connector Cap (M70), REF: 515406 BD PhaSeal Optima Injector (N35-O), REF: 515052 BD PhaSeal Optima Injector (N35-O Multi), REF: 515053 BD PhaSeal Injector Locking (N40-O), REF: 515056 BD PhaSeal Injector Locking (N40-O Multi), REF: 515057 BD PhaSeal Optima Protector (P13-O), REF: 515060 BD PhaSeal Optima Protector (P13-O Multi), REF: 515062 BD PhaSeal Optima Protector (P28-O), REF: 515063 BD PhaSeal Optima Protector (P20-O), REF: 515064 BD PhaSeal Optima Protector (P20-O Multi), REF: 515065 BD PhaSeal Optima Connector (C35-O), REF: 515070 BD PhaSeal Optima Infusion Adapter (C100-O), 515078 BD PhaSeal Optima Infusion Adapter (C100-O Multi), REF: 515079

Check your product

The notice names 18 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.

  • 00382905150036
  • 00382905150043
  • 00382905150050
  • 00382905151002
  • 00382905151026
  • 00382905151033
  • 00382905151040
  • 00382905151057

Model or item number

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

  • 515005 BD PhaSeal Protector
  • 515100 BD PhaSeal Protector
  • 515102 BD PhaSeal Protector
  • 515103 BD PhaSeal Protector
  • 515104 BD PhaSeal Protector
  • 515105 BD PhaSeal Protector
  • 515106 BD PhaSeal Protector
  • 515107 BD PhaSeal Protector
  • 515079 — REF
  • UDI-DI

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 Device

Bd Switzerland Sarl — This is a device enforcement record. Check whether the remedy is a correction, a software update or a removal before changing anything.

  1. Match the model, catalogue, lot and serial numbers on your device against the identifiers on this page.
  2. Ask the supplier or clinic that provided it what the remedy is in your case.
  3. If you are a facility, quarantine affected stock and log the correction.
  4. Report device problems to the FDA through MedWatch.

Replacements, repairs and reimbursement

Device remedies run through the supply chain, so the route depends on who sold you the unit.

  • Contact the distributor or clinic named on your paperwork and quote the recall number on this page. They will tell you whether the remedy is a repair, a replacement or an instruction update.
  • If the device was billed to insurance or Medicare, the replacement is usually billed the same way; you should not face a second deductible for a recall.
  • Keep every piece of correspondence. If a recalled device caused harm, that paper trail is what a claim rests on.
  • Consumer-purchased devices such as monitors and test kits are normally replaced free, with return shipping paid.

Company contact: BD SWITZERLAND SARL — Terre Bonne Park A4, Eysins

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 Bd Switzerland Sarl medical devices recalled?

Closed system drug transfer devices were shipped to the U.S. market without a U.S. version of the instructions for use, which could be an issue if a healthcare professional is prompted to review it. Closed system drug transfer devices were shipped to the U.S. market without a U.S. version of the instructions for use, which could be an issue if a healthcare professional is prompted to review it.

How do I know if I have the recalled product?

Match the codes printed on your package against the notice: UPC 00382905150036, 00382905150043, 00382905150050; model number 515005 BD PhaSeal Protector, 515100 BD PhaSeal Protector, 515102 BD PhaSeal Protector. 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?

Match the model, catalogue, lot and serial numbers on your device against the identifiers on this page.

Can I get my money back?

Contact the distributor or clinic named on your paperwork and quote the recall number on this page. They will tell you whether the remedy is a repair, a replacement or an instruction update.

Where was the recalled product sold?

It was distributed nationwide.

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