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Stryker Leibinger GmbH & Co. KG Botzinger Str. 41 Freiburg Im Breisgau Germany

Stryker Leibinger GmbH & Co. KG Botzinger Str. 41 Freiburg Im Breisgau Germany Recalls

All product recalls associated with Stryker Leibinger GmbH & Co. KG Botzinger Str. 41 Freiburg Im Breisgau Germany.

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Recall Summary

Total Recalls

1000

Past Year

888

Class I (Serious)

124

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 5221–5240 of 17593 recalls

DirectInject (Stryker) – Injection Difficulty (2021)

Inability for the user to inject the paste from the syringe into the target location.

Moderate

FDAApr 1, 2021Nationwide• Stryker Leibinger GmbH & Co. KG Botzinger Str. 41 Freiburg Im Breisgau Germany

Tranberg MR Cannula (Clinical Laserthermia) – Sterility Concern (2021)

single use devices labeled as sterile may not have been adequately sterilized

High

FDAApr 1, 2021Nationwide• CLINICAL LASERTHERMIA SYSTEMS AB Scheelevagen

Power Wheelchair (Merits) – Baseplate Pin Failure (2021)

Seat baseplate pin has broken in the field.

High

FDAApr 1, 2021Nationwide

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• Merits Holdings Co. dba Merits Health Products, Inc.

Tranberg MR Stylet (Clinical Laserthermia) – Sterility Concern (2021)

single use devices labeled as sterile may not have been adequately sterilized

High

FDAApr 1, 2021Nationwide• CLINICAL LASERTHERMIA SYSTEMS AB Scheelevagen

Scooter (Merits) – Baseplate Pin Failure (2021)

Seat baseplate pin has broken in the field.

High

FDAApr 1, 2021Nationwide• Merits Holdings Co. dba Merits Health Products, Inc.

Tranberg Laser Applicator (Clinical Laserthermia) – Sterility Concern (2021)

single use devices labeled as sterile may not have been adequately sterilized

High

FDAApr 1, 2021Nationwide• CLINICAL LASERTHERMIA SYSTEMS AB Scheelevagen

Itraconazole Capsules (Jubilant Cadista) - Failed Dissolution (2021)

Failed Dissolution Specifications

Class IIModerate

FDAApr 1, 2021Nationwide• Jubilant Cadista Pharmaceuticals, Inc.

AM12M Acquisition Module (Welch Allyn) – Compliance Issue (2021)

Devices do not meet IEC 60601-2-27 requirements as labeled.

Low

FDAMar 31, 2021Nationwide• Welch Allyn Inc Mortara

Surveyor S12/S19 Patient Monitor (Welch Allyn) – Compliance Issue (2021)

Devices do not meet IEC 60601-2-27 requirements as labeled.

Low

FDAMar 31, 2021Nationwide• Welch Allyn Inc Mortara

ELI 280 Electrocardiograph (Welch Allyn) – Compliance Issue (2021)

Devices do not meet IEC 60601-2-27 requirements as labeled.

Low

FDAMar 31, 2021Nationwide• Welch Allyn Inc Mortara

SoftCytogenetics (Soft Computer) – Incorrect Results (2021)

Software is given wrong results going out to HIS on test that had reruns.

Moderate

FDAMar 31, 2021Nationwide• Soft Computer Consultants, Inc.

SoftGenomics (Soft Computer) – Reporting Error (2021)

Software showing wrong results reported, PDF not match HIS.

Moderate

FDAMar 31, 2021CA• Soft Computer Consultants, Inc.

ELI 380 Electrocardiograph (Welch Allyn) – Compliance Issue (2021)

Devices do not meet IEC 60601-2-27 requirements as labeled.

Low

FDAMar 31, 2021Nationwide• Welch Allyn Inc Mortara

Cummins PD7000 (CUMMINS) – Electrical Protection Failure (2021)

Cummins, Inc. (Cummins) is recalling certain Electric Drivetrain part number PD7000. The electric drive train cannot detect isolation faults when the high voltage contactors are closed.

High

NHTSAMar 30, 2021Nationwide• CUMMINS

Calibration Serum Level 3 (Randox) – Bilirubin Bias (2021)

Randox can confirm a positive bias for Total Bilirubin and Direct Bilirubin of up to +15% across the assay ranges when using calibrator CAL2351, lot 1162UE. The positive bias has been attributed to bilirubin instability in the calibrator and is evident in both Quality Control (QC) and Patient samples.

Moderate

FDAMar 29, 2021CA, CT, IL +13 more• Randox Laboratories Ltd. 55 Diamond Road Crumlin (North) Ireland