Fresh Recalls

Stryker recalls

14 recent recalls on record for Stryker in connected official government data as of September 7, 2026 at 6:00 AM UTC.

Models with recalls

Neptune Smart Docking Station (120V) (1)STRYKER AHTO DUAL SPIKE TUBE SET PACKAGING (1)STRYKER AHTO TUBE SET PACKAGING (1)STRYKER AHTO TUBE SET WITH TIP PACKAGING (1)STRYKER PKG (2)Stryker Hoffmann II Connecting Rod Micro 3 x 120mm (1)Stryker Hoffmann II Connecting Rod Micro 3 x 150mm (1)Stryker Hoffmann II Connecting Rod Micro 3 x 30mm (1)Stryker Hoffmann II Connecting Rod Micro 3 x 40mm (1)Stryker Hoffmann II Connecting Rod Micro 3 x 50mm (1)Stryker Hoffmann II Connecting Rod Micro 3 x 60mm (1)Stryker Hoffmann II Connecting Rod Micro 3 x 90mm (1)Thermedx FluidSmart Urology Tube Set REF LL0006 UDI-DI code (1)

All Stryker recalls

FDA Class II · Medical device · August 12, 2026

STRYKER PKG recall — Stryker Corporation

There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.

Official ID Z-2866-2026 · Official record ↗

FDA Class II · Medical device · August 12, 2026

STRYKER PKG recall — Stryker Corporation

There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.

Official ID Z-2865-2026 · Official record ↗

FDA Class II · Medical device · August 12, 2026

STRYKER AHTO DUAL SPIKE TUBE SET PACKAGING recall — Stryker Corporation

There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.

Official ID Z-2864-2026 · Official record ↗

FDA Class II · Medical device · August 12, 2026

STRYKER AHTO TUBE SET WITH TIP PACKAGING recall — Stryker Corporation

There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.

Official ID Z-2863-2026 · Official record ↗

FDA Class II · Medical device · August 12, 2026

STRYKER AHTO TUBE SET PACKAGING recall — Stryker Corporation

There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.

Official ID Z-2862-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

Stryker Hoffmann II Connecting Rod Micro 3 x 150mm recall — Stryker GmbH

Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.

Official ID Z-2833-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

Stryker Hoffmann II Connecting Rod Micro 3 x 120mm recall — Stryker GmbH

Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.

Official ID Z-2832-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

Stryker Hoffmann II Connecting Rod Micro 3 x 90mm recall — Stryker GmbH

Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.

Official ID Z-2831-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

Stryker Hoffmann II Connecting Rod Micro 3 x 60mm recall — Stryker GmbH

Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.

Official ID Z-2830-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

Stryker Hoffmann II Connecting Rod Micro 3 x 50mm recall — Stryker GmbH

Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.

Official ID Z-2829-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

Stryker Hoffmann II Connecting Rod Micro 3 x 40mm recall — Stryker GmbH

Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.

Official ID Z-2828-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

Stryker Hoffmann II Connecting Rod Micro 3 x 30mm recall — Stryker GmbH

Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.

Official ID Z-2827-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

Neptune Smart Docking Station (120V) recall — Stryker Corporation

It has been identified that the impacted docking station (SN 2521008873) was not product released from manufacturing and may not have completed required testing prior to being ship…

Official ID Z-2282-2026 · Official record ↗

FDA Class II · Medical device · May 20, 2026

Thermedx FluidSmart Urology Tube Set REF LL0006 UDI-DI code recall — Stryker Corporation

Due to nonconforming products being inadvertently distributed.

Official ID Z-2166-2026 · Official record ↗

Verify with the official sources:

Found something wrong or missing? Report a data error.

Compiled from official public-domain government data. Last checked September 7, 2026 at 6:00 AM UTC.