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Waldemar Link GmbH & Co. KG (Mfg Site) Oststr. 4-10 Norderstedt Germany

Waldemar Link GmbH & Co. KG (Mfg Site) Oststr. 4-10 Norderstedt Germany Recalls

All product recalls associated with Waldemar Link GmbH & Co. KG (Mfg Site) Oststr. 4-10 Norderstedt Germany.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

143

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 4361–4380 of 37665 recalls

Embrace Drill Tower (Waldemar Link) – Technique Description Mix-up (2024)

The surgical techniques for the Embrace Shoulder Instruments -Drill Tower (Article REF 645-081/62 & /63) have mixed-up type descriptions ("standard" vs "wedged") in the overview of the instruments.

Low

FDAJan 29, 2024Nationwide• Waldemar Link GmbH & Co. KG (Mfg Site) Oststr. 4-10 Norderstedt Germany

Soltive Pro Laser (Olympus) – Non-Compliant Power Cord (2024)

A non-compliant power cord may have been supplied in regions that do not utilize the Type B or Type E/F plug configurations.

Low

FDAJan 29, 2024IN• Olympus Corporation of the Americas

Vantage Titan MRI (Canon) – SFG Value Mismatch (2024)

For some MRI systems, it has been found that some of the maximum Spatial Field Gradient (SFG) values displayed in "System Information" of the operation window and some of the maximum SFG values described in the safety manual are lower than the correct values, which may cause a patient with an MR conditional device to feel some discomfort during the MR scan.

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Moderate

FDAJan 29, 2024Nationwide• Canon Medical System, USA, INC.

IdentiTi ALIF System (Alphatec) – Graft Bolt Breakage (2024)

Due to reports of intraoperative graft bolt implantation breakages.

High

FDAJan 26, 2024Nationwide• Alphatec Spine, Inc. 1950 Camino Vida Roble

RNG International Battery Pack (RNG) – Relay Contactor Issue (2024)

Fire/Burn Risk

Renogy is recalling certain battery packs with model number RBT210LFP51S-12 and part number RBT210LFP51S-12-G1-U. The battery relay contactors may become stuck in the closed position.

High

NHTSAJan 26, 2024Nationwide• RNG INTERNATIONAL

I.B.S Compression Screw (In2Bones) – Batch Mix-up (2024)

This Field Action is being conducted following the identification of a batch mix-up between I.B.S Compression screws diameter 6.5mm length 75mm and I.B.S Compression screws diameter 6.5mm length 80mm. The screws of the batches concerned by the recall may have different lengths from those issued on their labels.

Moderate

FDAJan 26, 2024Nationwide• In2Bones, SAS 28 Chemin du petit Bois Ecully France

IonoStar Plus (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.

Moderate

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

Terex Advance HRX55 (Terex) – Boom Rotation Bolt Failure (2024)

Terex South Dakota, Inc. (Terex) is recalling certain 2023 Optima-TC55, Optima-HRX50, Optima-HRX55, and XT Pro vehicles. The boom rotation bearing bolts may not be tightened properly.

High

NHTSAJan 25, 2024Nationwide• TEREX ADVANCE

Peterbilt 567 (Peterbilt) – Steering Defect (2024)

PACCAR Incorporated (PACCAR) is recalling certain 2024-2025 Kenworth T280, T380, T480, T680, T880, L770, W990, and 2024-2025 Peterbilt 389, 520, 535, 536, 537, 548, 567, 579, 589 trucks. The steering gear assemblies may have been assembled incorrectly with fewer recirculating balls than are required, which may result in a loss of steering control.

High

NHTSAJan 25, 2024Nationwide• PETERBILT

Ionolux (Voco) – Plunger Fitting Error (2024)

Moderate

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

Peterbilt 520 (Peterbilt) – Bearing Journal Issue (2024)

PACCAR Incorporated (PACCAR) is recalling certain 2024 Peterbilt 367, 389, 520, 567, and Kenworth T800, T880, W900, and W990 trucks. The bearing journals may not be fully seated in the steering knuckle assemblies, preventing the proper installation of the wheel end hub assemblies.

High

NHTSAJan 25, 2024Nationwide• PETERBILT

Morning Glory Muffins (Lunds Mitchell) – Foreign Material (2024)

Foreign material (metal)

Class IIModerate

FDAJan 25, 2024MN• Lunds Mitchell Rd LLC

Nortrel Tablets (Teva) – Tablet Discoloration (2024)

Discoloration: discolored tablets (shades of blue) mixed in with the white inert remainder tablets.

Class IIILow

FDAJan 25, 2024Nationwide• Teva Pharmaceuticals USA, Inc

Febuxostat Tablets (Amerisource) – CGMP Deviation (2024)

CGMP Deviations

Class IIModerate

FDAJan 25, 2024Nationwide• Amerisource Health Services LLC

Nortrel 7/7/7 Tablets (Teva) – Tablet Discoloration (2024)

Discoloration: discolored tablets (shades of blue) mixed in with the white inert remainder tablets.

Class IIILow

FDAJan 25, 2024Nationwide• Teva Pharmaceuticals USA, Inc

RAPIDSORB IPS Battery Pack (Synthes) – Sterility Concerns (2024)

Products not sterilized, sterility cannot be confirmed

High

FDAJan 24, 2024Nationwide• Synthes (USA) Products LLC

Opal Intervertebral Cage (Synthes) – Sterility Concerns (2024)

Products not sterilized, sterility cannot be confirmed

High

FDAJan 24, 2024Nationwide• Synthes (USA) Products LLC

Atellica IM EPO Assay (Siemens) – Result Bias (2024)

Siemens Healthcare Diagnostics has confirmed an average negative bias of -35% compared to the 3rd World Health Organization (WHO) International Standard (NIBSC code: 11/170) that is proportional across the assay measuring interval. The reference interval as claimed in the Instructions for Use (IFU) is not achieved with affected lots.

Moderate

FDAJan 24, 2024Nationwide• Siemens Healthcare Diagnostics, Inc.

Impression Coping (Thommen) – Canal Depth Issue (2024)

The depth of the internal canal was not manufactured according to specifications. Thus, the impression coping cannot be firmly connected to the implant.

Low

FDAJan 24, 2024Nationwide• Thommen Medical AG Eschenweg 3 Bettlach Switzerland

TFNA Femoral Nail 9mm (Synthes) – Sterility Concerns (2024)

Products not sterilized, sterility cannot be confirmed

High

FDAJan 24, 2024Nationwide• Synthes (USA) Products LLC