medical MODERATE Updated 2026-09-23

Boston Scientific Corporation recalls Boston Scientific Corporation StoneSmart Connect Console C

See all recalls from Boston Scientific Corporation →

Recalled Product

Boston Scientific Corporation StoneSmart Connect Console Contents: (1) Power Cord, (1) Power Adaptor, (1)DVI Cable, (1) DVI to HDMI Cable, (1) DisplayPort Cable REF: M0067933000, M006793300H0, M006793300R0, M006793300D0, M006793300Z0, M0067930000, M006793000R0

Share this recall: Facebook X / Twitter WhatsApp Email

Hazard / Issue

A subset of power adapters used with the connect console may exhibit higher-than-expected resistance in the electrical grounding path. As a result, the power adaptor may fail electrical safety testing during installation.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: All Serial Numbers: REF: M0067933000 (UDI 00191506002510, UDI (00191506021771); REF: M006793300H0 (UDI 00191506002558); REF: M006793300R0 (UDI 00191506002534), UDI (00191506021788); REF: M006793300D0 (UDI 00191506002527); REF: M006793300Z0 (UDI 00191506002541); UPN M0067933100 (UDI 00191506022549)

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

Looking for a safe alternative?

Search Amazon for Boston Scientific Corporation →

If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.

View official government recall

Related medical Recalls

Medline Industries, LP recalls Convenience kits CATARACT PACK DYNJ59881A

2026-09-23 · Kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to contamination of sterile field or patient infection if product is used.

Bard Access Systems, Inc. recalls DuoGlide Short-Term Straight Dialysis Catheter, REF: 5625150

2026-09-23 · this is a downstream recall of class I recall RES 98777

Maquet Cardiopulmonary Gmbh recalls Percutaneous Insertion Kit (PIK), dilator set L, Model Numbe

2026-09-23 · The packaging may not consistently maintain sterile barrier integrity.

Medical Action Industries, Inc. 306 recalls Blood Culture Collection Venipuncture Kit 20/Cs, REF: 77451;

2026-09-23 · Blood culture convenience kits contain a component subject to a drug recall that due to an an open or incomplete seal on the packaging of the applicator may compromise the component's sterile barrier and if used may lead to localized skin or soft tissue infection.