Stay Informed

Get email alerts when new recalls match your interests.

Recall data is updated hourly from official government sources. Very recent recalls may not yet appear. About our data sources

About

We make U.S. recall data searchable and accessible for consumers and businesses.

Site

FAQ
Browse by State
Statistics
Recall Classifications
About
Enterprise API

Legal

Privacy Policy
Terms of Service
Report Incorrect Info

Official Sources

FDA Recalls ↗
USDA FSIS ↗
CPSC Recalls ↗
NHTSA Recalls ↗

RSS Feed

Home
/
Brands
/
Aesculap AG Am Aesculap-Platz 1 Tuttlingen Germany

Aesculap AG Am Aesculap-Platz 1 Tuttlingen Germany Recalls

All product recalls associated with Aesculap AG Am Aesculap-Platz 1 Tuttlingen Germany.

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

426

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 181–200 of 4598 recalls

Aesculap Elan 4 Duraguard (Aesculap) – Mislabeling Issue (2025)

Mislabeling. The ELAN 4 FIXED DURAGUARD STANDARD was labeled as "Long" and the ELAN 4 FIXED DURAGUARD LONG was labeled as "Standard."

Low

FDAAug 18, 2025MO• Aesculap AG Am Aesculap-Platz 1 Tuttlingen Germany

Volkswagen Tiguan (Volkswagen) – Tie Rod Bolt Issue (2025)

Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2025 Tiguan vehicles. A tie rod bolt on the rear axle assembly may be loose, which can lead to a loss of vehicle control.

High

NHTSAAug 13, 2025Nationwide• VOLKSWAGEN

Change Healthcare Radiology Software (Change Healthcare) – Report Display Issue (2025)

Due to software issue, radiology reports may not be fully displayed when viewing.

Low

FDAAug 13, 2025

1...8 91011 12...230

Page 10 of 230Next

Nationwide

• CHANGE HEALTHCARE CANADA COMPANY

Merge Hemo Software (Merge Healthcare) – patient data issue (2025)

Merge Healthcare has been informed by Schiller AG (Baar, Switzerland) of an issue with the Schiller ARGUS PB-3000 Patient Data Module (PDM) where certain units trigger an error message on the Merge Hemo Client (Pressure Sensor Defective) during non-invasive blood pressure (NIBP) measurements, specifically when the initial inflation pressure is set in the high-pressure range (>240 mmHg). The ARGUS PB-3000 is a vital signs monitoring instrument intended to be integrated into the Merge Hemo System. No other components of the Merge Hemo System are affected.

Moderate

FDAAug 11, 2025Nationwide• Merge Healthcare, Inc.

RayStation Software (RaySearch) – UID uniqueness (2025)

DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the interface to Accuray's iDMS, are not guaranteed to be unique.

Low

FDAAug 8, 2025Nationwide• RAYSEARCH LABORATORIES AB Eugeniavagen 18c Stockholm Sweden

Duloxetine Capsules (Breckenridge) - CGMP Impurity (2025)

CGMP deviations: N-nitroso-duloxetine impurity above the proposed interim limit.

Class IIModerate

FDAAug 8, 2025AZ, IN, NJ• Breckenridge Pharmaceutical, Inc.

LinkSymphoKnee System (Waldemar Link) – screw issue (2025)

Some modular LinkSymphoKnee TiNbN Tibial Components were manufactured with two uncoated security screws, which is incorrect.

Low

FDAJul 31, 2025Nationwide• Waldemar Link GmbH & Co. KG (Mfg Site) Oststr. 4-10 Norderstedt Germany

Fortress Introducer Sheath (Contract Medical) – labeling error (2025)

Units may have been packaged with an incorrect pouch label, which lists the reference number and unique device identifier of the 4F version of the device, rather than the packaged 6F version.

Low

FDAJul 30, 2025Nationwide• Contract Medical International GmbH Lauensteiner Str. 37 Dresden Germany

Clover Valley Instant Coffee (Dollar General) – glass pieces risk (2025)

Potential presence of glass pieces

Class IIModerate

FDAJul 27, 2025AL, AZ, AR +45 more• Dollar General Corporation

Duloxetine Capsules (Breckenridge) – Nitrosamine Impurity (2025)

CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit.

Class IIModerate

FDAJul 25, 2025AZ, IN, NJ• Breckenridge Pharmaceutical, Inc.

Gelson's Tzatziki – missing storage instructions (2025)

Gelson branded Tzatziki sauce product labels do not include storage instructions "keep refrigerated"

Class IIModerate

FDAJul 25, 2025CA, IN• Gelsons

Gelson's Mediterranean Hummus – missing storage instructions (2025)

Gelson branded Hummus product labels do not include storage instructions "keep refrigerated"

Class IIModerate

FDAJul 25, 2025CA, IN• Gelsons

Gelson's Low Sodium Hummus – missing storage instructions (2025)

Gelson branded Hummus product labels do not include storage instructions "keep refrigerated"

Class IIModerate

FDAJul 25, 2025CA, IN• Gelsons

Gelson's Hummus – missing storage instructions (2025)

Gelson branded Hummus product labels do not include storage instructions "keep refrigerated"

Class IIModerate

FDAJul 25, 2025CA, IN• Gelsons

Georgia Pine Turpentine (Diamond G) – ingestion risk (2025)

This recall involves 100% pure gum spirits of turpentine bottles. The 4-ounce, clear glass bottles are round and have a label with "Georgia Pine Gum Spirits of Turpentine" and "Diamond G Forest Products" printed on it.

High

CPSCJul 24, 2025Nationwide• Diamond G Forest Products LLC, of Patterson, Georgia

Genesis GV60 (Genesis) – Instrument Panel Error (2025)

Hyundai Motor America (Hyundai) is recalling certain Genesis 2023-2025 G90 and GV60 vehicles. Due to a software error, the instrument panel display may fail. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 101, "Controls and Displays."

High

NHTSAJul 17, 2025Nationwide• GENESIS

Prosthesis Head B (Waldemar Link) – Labeling Inconsistency (2025)

Inconsistent size terminology and color coding used on labeling

Moderate

FDAJul 15, 2025Nationwide• Waldemar Link GmbH & Co. KG (Mfg Site) Oststr. 4-10 Norderstedt Germany

Plastic Trial Head (Waldemar Link) – Labeling Inconsistency (2025)

Inconsistent size terminology and color coding used on labeling

Moderate

FDAJul 15, 2025Nationwide• Waldemar Link GmbH & Co. KG (Mfg Site) Oststr. 4-10 Norderstedt Germany

General Tire Altimax RT45 (General Tire) – Overcuring Problem (2025)

Continental Tire the Americas, LLC (CTA) is recalling certain General Tire Altimax RT45 tires, size 235/60R18. The tires may have been overcured during manufacturing.

High

NHTSAJul 15, 2025Nationwide• GENERAL TIRE

Duloxetine Capsules (Breckenridge Pharmaceutical) – Impurity Concern (2025)

CGMP Deviations: Presence of N-nitroso-duloxetine impurity above safety assessment limit

Class IIModerate

FDAJul 15, 2025Nationwide• Breckenridge Pharmaceutical, Inc.