Class III U.S. Food and Drug Administration

Philips Ultrasound, Inc X6-1 Transducer Probe recall: To provide clarification and labelling to define the useful life

Recall published 1+ years ago

To provide clarification and labelling to define the useful life of ultrasound transducers in the field.

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: To provide clarification and labelling to define the useful life of ultrasound transducers in the field.

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-2410-2025
Published
September 3, 2025
Risk level
Class III
Status
Ongoing
Issued by
U.S. Food and Drug Administration
Brand
Philips Ultrasound, Inc
Product type
Medical devices
Units affected
171,322 units
Distribution
Nationwide
Made in
United States
Lot / code info
Model No. 989605409282, 989605438511, 989605357141, 989605357143, 989605427801; UDI: (01)00884838061446(21)B22RP6, (01)00884838061446(21)F01N54, (01)00884838061446(21)B28KXP, (01)00884838061446(21)B2HRV1, (01)00884838061446(21)F0HR2C, (01)00884838061446(21)B2K24P, (01)00884838061446(21)B2L7JQ, (01)00884838061446(21)B3D77Q, (01)00884838061446(21)F02MHJ, (01)00884838061446(21)B21DYX, (01)00884838061781(21)B1Z20M, (01)00884838061781(21)B22QTZ, (01)00884838061781(21)B26888, (01)00884838061781(21)B28KXF, (01)00884838061446(21)B29X6N, (01)00884838061446(21)B37K59, (01)00884838061446(21)B2F0XT, (01)00884838061781(21)B305VR, (01)00884838061781(21)B3BPQL, (01)00884838061446(21)F0CFRQ, (01)00884838061446(21)B2L8ZT, (01)00884838061446(21)B1JBW3, (01)00884838061446(21)B1JD06, (01)00884838061446(21)B1JFHH, (01)00884838061446(21)F00PZJ, (01)00884838061446(21)B29Y6B, (01)00884838061446(21)B2RWK0, (01)00884838061446(21)B305W1, (01)00884838061446(21)B1JCTV, (01)00884838061446(21)F04123, (01)00884838061446(21)F0DDD7, (01)00884838061446(21)F09980, (01)00884838061446(21)F09Y27, (01)00884838061446(21)F02G1Q, (01)00884838061446(21)B28HZ1, (01)00884838061446(21)B28KXB, (01)00884838061446(21)B2K9WV, (01)00884838061446(21)B1JC08, (01)00884838061446(21)B1JCTW, (01)00884838061446(21)B1JCXY, (01)00884838061446(21)B2FC7Y, (01)00884838061781(21)B27YFD, (01)00884838061446(21)F00HW1, (01)00884838061446(21)B2B3JB, (01)00884838061446(21)B2D297, (01)00884838061446(21)B2DYJC, (01)00884838061446(21)F02RT6, (01)00884838061446(21)F008BK, (01)00884838061446(21)F03BX0, (01)00884838061446(21)B21CGX, (01)00884838061446(21)B241J8, (01)00884838061446(21)B241JH, (01)00884838061446(21)B24V6Q, (01)00884838061446(21)B24VMJ, (01)00884838061446(21)B24VXW, (01)00884838061446(21)B24VY5, (01)00884838061446(21)B2R02Z, (01)00884838061446(21)F01QZQ, (01)00884838061446(21)F030R2, (01)00884838061446(21)F07246, (01)00884838061446(21)F03W54, (01)00884838061446(21)B3TX0H, (01)00884838061446(21)B2K25C, (01)00884838061446(21)F07XFG, (01)00884838061446(21)B1YFRP, (01)00884838061446(21)B22RNZ, (01)00884838061446(21)B24DRK, (01)00884838061446(21)B21DFQ, (01)00884838061446(21)B29Y6F, (01)00884838061446(21)F074QN, (01)00884838061446(21)B2X6N3, (01)00884838061446(21)B3KZL5, (01)00884838061446(21)B3KZLD, (01)00884838061446(21)F01DHZ, (01)00884838061446(21)F01J13, (01)00884838061446(21)B22QVK, (01)00884838061446(21)B21CGZ, (01)00884838061446(21)B28277, (01)00884838061446(21)F0BHX1, (01)00884838061446(21)F04121, (01)00884838061781(21)B22F70, (01)00884838061446(21)B1J2H4, (01)00884838061446(21)B21DKQ, (01)00884838061446(21)B21F0D, (01)00884838061446(21)B21W57, (01)00884838061446(21)B2J327, (01)00884838061446(21)F0D7RJ, (01)00884838061446(21)B2DJV6, (01)00884838061446(21)B2GYLV, (01)00884838061446(21)B2GYLZ, (01)00884838061446(21)B2GYM1, (01)00884838061446(21)B2GYM6, (01)00884838061446(21)B37K6F, (01)00884838061446(21)F0G8HF, (01)00884838061446(21)B25DTH, (01)00884838061446(21)B28M4K, (01)00884838061446(21)B2KB4C, (01)00884838061446(21)F0050L, (01)00884838061446(21)F0050M, (01)00884838061446(21)F0050Q, (01)00884838061781(21)B27YN7, (01)00884838061446(21)B1JD04, (01)00884838061446(21)B2HRV0, (01)00884838061446(21)B2X6N2, (01)00884838061446(21)B305TY, (01)00884838061446(21)B1J6R0, (01)00884838061446(21)B28KXM, (01)00884838061446(21)B2929V, (01)00884838061446(21)B2B3JC, (01)00884838061446(21)B2K9MB, (01)00884838061446(21)B2KHN3, (01)00884838061446(21)B2KB46, (01)00884838061446(21)B2KC4N, (01)00884838061446(21)B2KFGR, (01)00884838061446(21)B2KFL0, (01)00884838061446(21)F0BB0T, (01)00884838061446(21)F0BBYT, (01)00884838061446(21)F0BBYW, (01)00884838061446(21)F0C94Y, (01)00884838061446(21)F0CFRR, (01)00884838061446(21)F0CPGR, (01)00884838061446(21)B1GVNY, (01)00884838061446(21)B2J32B, (01)00884838061446(21)B37K50, (01)00884838061446(21)B2DZ2N, (01)00884838061446(21)B3B1XR, (01)00884838061446(21)F054CZ, (01)00884838061446(21)F06D71, (01)00884838061446(21)B2RBH2, (01)00884838061446(21)B2B4N8, (01)0088483806…
UPC codes
989605409282, 989605438511, 989605357141, 989605357143, 989605427801, 00884838061446, 00884838061781

Products covered by this recall

X6-1 Transducer Probe

Check your product

The notice names 12 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.

  • 989605409282
  • 989605438511
  • 989605357141
  • 989605357143
  • 989605427801
  • 00884838061446
  • 00884838061781

Model or item number

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

  • 989605409282
  • 989605438511
  • 989605357141
  • 989605357

Package size

Match the net weight or the piece count on the front of the pack.

  • 0050 L

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

Philips Ultrasound, Inc — 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. If the device is implanted or you depend on it daily, speak to your clinician before changing how you use it.
  3. Ask the supplier or clinic that provided it what the remedy is in your case.
  4. If you are a facility, quarantine affected stock and log the correction.

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: Philips Ultrasound, Inc — 1 Echo Dr, Reedsville, PA, 17084-8603

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 Philips Ultrasound, Inc medical devices recalled?

To provide clarification and labelling to define the useful life of ultrasound transducers in the field. To provide clarification and labelling to define the useful life of ultrasound transducers in the field.

How do I know if I have the recalled product?

Match the codes printed on your package against the notice: UPC 989605409282, 989605438511, 989605357141; model number 989605409282, 989605438511, 989605357141. 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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