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Smith & Nephew Orthopaedics GmbH Alemannenstr. 14 Tuttlingen Germany

Smith & Nephew Orthopaedics GmbH Alemannenstr. 14 Tuttlingen Germany Recalls

All product recalls associated with Smith & Nephew Orthopaedics GmbH Alemannenstr. 14 Tuttlingen Germany.

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Recall Summary

Total Recalls

1000

Past Year

590

Class I (Serious)

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 2681–2700 of 10391 recalls

INTERTAN Nail (Smith & Nephew) – left-right labeling error (2022)

Right nails were anodized, marked, and labelled as left nails and vice versa

FDAApr 22, 2022Nationwide• Smith & Nephew Orthopaedics GmbH Alemannenstr. 14 Tuttlingen Germany

Locking Cap (Baxter) – regulatory clearance issue (2022)

Certain Peritoneal Dialysis product codes do not have FDA regulatory clearance and were distributed within the United States in error.

FDAApr 21, 2022Nationwide• Baxter Healthcare Corporation

5 Prong Manifold Set (Baxter) – regulatory clearance issue (2022)

Certain Peritoneal Dialysis product codes do not have FDA regulatory clearance and were distributed within the United States in error.

FDA

1...133 134135136 137...520

Page 135 of 520Next

Apr 21, 2022

Nationwide

• Baxter Healthcare Corporation

15 Liters Drain Bag (Baxter) – regulatory clearance issue (2022)

Certain Peritoneal Dialysis product codes do not have FDA regulatory clearance and were distributed within the United States in error.

FDAApr 21, 2022Nationwide• Baxter Healthcare Corporation

Effluent Sample Bag (Baxter) – regulatory clearance issue (2022)

Certain Peritoneal Dialysis product codes do not have FDA regulatory clearance and were distributed within the United States in error.

FDAApr 21, 2022Nationwide• Baxter Healthcare Corporation

ProudP Uroflow Tracker (Dain Technology) – sound processing issue (2022)

Due to interference with the Live Listen feature of hearing aid or AirPods, the user's iPhone may perform automatic processing of the urination sound signal, resulting in lower urination volume and velocity values than expected.

FDAApr 21, 2022Nationwide• Dain Technology, Inc. (Subsidiary of Soundable Health, Inc.) Seocho-Daero, Seocho # 413 398 Platinum Tower Seoul Korea (the Republic of)

APD Drain Manifold (Baxter) – regulatory clearance issue (2022)

Certain Peritoneal Dialysis product codes do not have FDA regulatory clearance and were distributed within the United States in error.

FDAApr 21, 2022Nationwide• Baxter Healthcare Corporation

Extension Set (Baxter) – regulatory clearance issue (2022)

Certain Peritoneal Dialysis product codes do not have FDA regulatory clearance and were distributed within the United States in error.

FDAApr 21, 2022Nationwide• Baxter Healthcare Corporation

C304-HIS Device (Medtronic) – sterility barrier concern (2022)

The firm's internal processes identified that certain lots may have an improperly sealed barrier that could potentially compromise sterility.

FDAApr 20, 2022Nationwide• Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Legion Narrow Knee Implant (Smith & Nephew) – mislabeling (2022)

It was reported that a JOURNEY II BCS Femoral OXIN LT SZ5 was in a box labelled as a LEGION NARROW PS OXIN SZ 6N RT.

FDAApr 19, 2022Nationwide• Smith & Nephew Inc

GE Ventilator Batteries (GE Healthcare) – backup power issue (2022)

Insufficient battery backup power resulting in premature shutdown of the ventilator when not connected to AC mains power supply.

FDAApr 18, 2022Nationwide• GE Healthcare, LLC

GE Replacement Batteries (GE Healthcare) – backup power issue (2022)

Insufficient battery backup power resulting in premature shutdown of the ventilator when not connected to AC mains power supply.

FDAApr 18, 2022Nationwide• GE Healthcare, LLC

Tacrolimus Suspension (Valor Compounding) – Subpotent Drug (2022)

Subpotent drug

Class IHigh

FDAApr 15, 2022CA• Valor Compounding Pharmacy, Inc DBA Valor Compounding Pharmacy

AUTOLITH Touch Lithotripter (Northgate) – Incorrect Labeling (2022)

Product labeled incorrectly.

FDAApr 13, 2022Nationwide• Northgate Technologies, Inc.

Atellica IM 1300 Analyzer (Siemens) – Erroneous T3 Results (2022)

Lots incompatible with Test Definition (TDef) Version 1.4, potentially lead to the generation of erroneous total T3 results

FDAApr 13, 2022Nationwide• Siemens Healthcare Diagnostics, Inc.

Atellica IM 1600 Analyzer (Siemens) – Erroneous T3 Results (2022)

Lots incompatible with Test Definition (TDef) Version 1.4, potentially lead to the generation of erroneous total T3 results

FDAApr 13, 2022Nationwide• Siemens Healthcare Diagnostics, Inc.

Voalte Nurse Call System (Baxter) – Firmware Memory Leak (2022)

Firm discovered a firmware memory leak with a supplier-manufactured component.

FDAApr 13, 2022NC, VA• Baxter Healthcare Corporation

NaviCare Nurse Call System (Baxter) – Firmware Memory Leak (2022)

Firm discovered a firmware memory leak with a supplier-manufactured component.

FDAApr 13, 2022NC, VA• Baxter Healthcare Corporation

Cobalt Cardiac Device (Medtronic) – Telemetry Error (2022)

Telemetry error that may occur with Medtronic Cobalt and Crome implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators (CRT-Ds).

FDAApr 12, 2022Nationwide• Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Crome Cardiac Device (Medtronic) – Telemetry Error (2022)

Telemetry error that may occur with Medtronic Cobalt and Crome implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators (CRT-Ds).

FDAApr 12, 2022Nationwide• Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)