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Voco GmbH Anton-Flettner-Str. 1-3 Cuxhaven Germany

Voco GmbH Anton-Flettner-Str. 1-3 Cuxhaven Germany Recalls

All product recalls associated with Voco GmbH Anton-Flettner-Str. 1-3 Cuxhaven Germany.

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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 701–720 of 4598 recalls

Ionolux (Voco) – Plunger Fitting Error (2024)

Due to an error in the manufacturing process, it is possible that an incorrect plunger has been fitted to some capsules. This plunger does not contain the correct reactive component for Ionolux. When these capsules are activated, curing is significantly delayed and incomplete. Processing according to the instructions for use is not possible.

FDAJan 25, 2024IA, NY, PA +1 more• Voco GmbH Anton-Flettner-Str. 1-3 Cuxhaven Germany

IonoStar Plus (Voco) – Plunger Fitting Error (2024)

FDAJan 25, 2024IA, NY, PA +1 more• Voco GmbH Anton-Flettner-Str. 1-3 Cuxhaven Germany

Battery Mobile X-ray Unit (Sedecal) – Anti-Fall System Interference (2024)

Potential interference with the anti-fall system.

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FDAJan 22, 2024Nationwide• SEDECAL SA PELAYA, 9 POL. POL. IND. RIO DE JANEIRO Algete Spain

Duet External Drainage System (Medtronic) – Catheter Disconnection Risk (2024)

Potential for catheter disconnection from the patient line stopcock connectors.

FDAJan 22, 2024Nationwide• Medtronic Neurosurgery

BiMobile Dual Mobility System (Waldemar Link) – Mislabeling Risk (2024)

Mislabeled: Packaging incorrectly reflects a MobileLink Dual Mobility insert type F when it should reference G may cause a delay in surgery

FDAJan 22, 2024Nationwide• Waldemar Link GmbH & Co. KG (Mfg Site) Oststr. 4-10 Norderstedt Germany

5 Grain Cereal (Woodstock) – wheat not identified (2024)

The ingredient Triticale is not identified as wheat.

Class IIModerate

FDAJan 18, 2024Nationwide• UNFI General Corporate

Furniture Tip Restraints (New Age) – Safety Risk (2024)

This recall involves plastic New Age furniture tip restraint kits that were sold and distributed by various furniture companies with clothing storage units. Participating Furniture Companies American Drew American Woodcrafters Amini Innovation Corporation Ashley Furniture Industries, LLC Aspenhome Austin Group Furniture, LLC Avalon International Inc., LLC Bassett Furniture Industries, Inc. Drew and Jonathan by Hooker Furnishings Emery Park FD Home Corp. Flexsteel Industries, Inc. Furniture Values International, LLC Homelegance USA, LLC Hooker Furnishings Kincaid Furniture LC Direct Furniture Legacy Classic/Modern Furniture Liberty Furniture Industries, Inc. Magnussen Home Furnishings, Inc. New Classic Home Furnishings, Inc. Parker House Furniture Progressive Furniture Pulaski Furniture Riverside Furniture Samuel Lawrence Springhill Designs Standard Furniture Manufacturing Co., LLC Universal Furniture Van Thiel & Co. Vanguard Furniture Company. The New Age tip restraint kits included a plastic zip-tie, two brackets, and two screws and were sold with clothing storage units manufactured in Vietnam. The date of manufacture should be listed on a sticker or stamped on the clothing storage unit as November 2019 or later. The packaging of the recalled tip kits is white with black lettering and includes directions on how to anchor furniture. The bottom of the packaging states "Manufactured by New Age Industries."

CPSCJan 11, 2024Nationwide• New Age Industries Co. LTD, of Vietnam

Custodiol HTK Solution (Dr. Franz Koehler) – Particle Presence (2024)

Potential for particles to be present in solution.

FDAJan 9, 2024Nationwide• Dr Franz Koehler Chemie Gmbh Werner-Von-Siemens-Str. 14-28 Bensheim Germany

GE Lullaby Incubator (GE Healthcare) – bedside panel issue (2023)

GE HealthCare has become aware that the bedside panel of Care Plus, Care Plus Model 1000, 2000, 3000 and 4000 Incubator, Lullaby Incubator, Lullaby TR Incubator, and Lullaby XP Incubator can be upright and look closed but not be latched if the red indicator is visible. The portholes also can look closed when not latched when the portholes are obstructed e.g., hood covers. If a patient impacts the bedside panel or porthole that is not latched, the panel can disengage and fall open, no longer protecting the patient from falling.

FDADec 26, 2023Nationwide• Wipro GE Healthcare Private Ltd. 122 Part 1 Odyssey And Galileo Bengaluru India

GE Neonatal Incubator (GE Healthcare) – bedside panel problem (2023)

FDADec 26, 2023Nationwide• Wipro GE Healthcare Private Ltd. 122 Part 1 Odyssey And Galileo Bengaluru India

GE Care Plus Hood (GE Healthcare) – bedside panel issue (2023)

FDADec 26, 2023Nationwide• Wipro GE Healthcare Private Ltd. 122 Part 1 Odyssey And Galileo Bengaluru India

Senographe Pristina (GE Medical Systems) – x-ray signal issue (2023)

X-ray exposure termination audible signal on Senographe Pristina with Efficiency Suite 2 intermittently not emitted per 21CFR 1020.31(j) requirements.

FDADec 26, 2023Nationwide• GE Medical Systems, SCS

GE Voluson Probe (GE Healthcare) – image artifact risk (2023)

GE HealthCare has become aware of an issue with certain IC9-RS ultrasound probes (see Affected Products List) that can result in a double image artifact creating a ghost image with realistic features. An unrecognized artifact may lead to misdiagnosis.

FDADec 22, 2023Nationwide• GE HEALTHCARE AUSTRIA GMBH & CO Tiefenbach 15 Pfaffing Austria

Rebstock Holding Rod (Medagent) – uncontrolled movement risk (2023)

Holding arm could move (twist) uncontrollably in the front area. This could lead to a serious deterioration of patient's safety if the movement is transferred to the spatula, which is attached to the holding arm.

FDADec 21, 2023TX• Medagent Inc

Americaine Benzocaine Spray (Insight) – Benzene Contamination (2023)

Chemical Contamination: presence of benzene

Class IHigh

FDADec 21, 2023Nationwide• Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company

Accessory Set Syringes (OriGen) – Qualification Concern (2023)

Accessory sets contain a syringes not yet qualified for the accessory's intended purpose; due to design changes to the syringe barrels and a polypropylene resin change that resulted in loss of gamma compatibility, for accessory set syringes that were gamma sterilized, which resulted in yellowed syringes.

FDADec 19, 2023CA, DE, FL +8 more• OriGen Biomedical, Inc.

Sedecal X Optima URS X-Ray (Sedecal) – Equipment Part Failure (2023)

Some parts have fallen off the equipment resulting in a safety risk to patients and/or users.

FDADec 13, 2023AL, FL, NC• SEDECAL SA PELAYA, 9 POL. POL. IND. RIO DE JANEIRO Algete Spain

Flow-c Anesthesia System (Getinge) – Cybersecurity Vulnerability (2023)

Laceration Risk

Potential cybersecurity vulnerability that could lead to a Denial of Service (DoS) attack, tampering, or remote code execution via remote login to the Flow Anesthesia System, any of which could lead to a hazardous situation.

FDADec 11, 2023Nationwide• Getinge Usa Sales Inc

Flow-i C20 Anesthesia System (Getinge) – Cybersecurity Vulnerability (2023)

Laceration Risk

FDADec 11, 2023Nationwide• Getinge Usa Sales Inc

Flow-i C40 Anesthesia System (Getinge) – Cybersecurity Vulnerability (2023)

Laceration Risk

FDADec 11, 2023Nationwide• Getinge Usa Sales Inc