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Micro Labs Limited

Micro Labs Limited Recalls

All product recalls associated with Micro Labs Limited.

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Recall Summary

Total Recalls

1000

Past Year

583

Class I (Serious)

Most Recent

Dec 2025

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 1141–1160 of 10937 recalls

Clobazam Tablets (Micro Labs) – Residual Solvent Issue (2024)

CGMP Deviations: Out of specification for residual solvents.

Class IIModerate

FDAFeb 12, 2024Nationwide• Micro Labs Limited

Telmisartan Tablets (Micro Labs) – Blend Uniformity Issue (2024)

Failed Stability Specifications: Out of specification for blend uniformity.

Class IIModerate

FDAFeb 9, 2024RI, TN, PR• Micro Labs Limited

VERIQA Software (PTW-Freiburg) – Gamma Calculation Issue (2024)

Software: If the user excludes voxels from the Gamma calculation that are below a dose threshold (Suppress gamma calculation), the Gamma Passing Rate (GPR) calculated for individual ROIs is not correct. The GPR calculated by VERIQA overestimates the correct GPR. The evaluation can therefore show false positive results.

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FDAFeb 8, 2024GA• PTW-FREIBURG Lorracher Str. 7 Freiburg Im Breisgau Germany

Children's Bathrobes (Lolanta) – Burn Hazard (2024)

Fire/Burn Risk

This recall involves two styles of 100% polyester hooded children's bathrobes; the dinosaur style in green, rose red and orange, and the shark style in blue, pink, yellow and gray. The bathrobes have attached belts and patch pockets. The size, manufacturer information and care instructions are printed on sewn-in labels inside the left inseam of the robes. They were sold in sizes 2-3 years, 3-5 years, and 6-8 years.

CPSCFeb 8, 2024Nationwide• Nanchang Zhongcangjishi E-commerce Co. Ltd, of China

DLP Vessel Cannula (Medtronic) – Labeling Error (2024)

Medtronic is writing to inform you of incorrect labeling for three manufactured lots of the DLP Vessel Cannulae for the model and lot numbers listed above.

FDAFeb 7, 2024GA• Medtronic Perfusion Systems

Azurion 5 (Philips) – Generator Failure Risk (2024)

Generator may fail due to a potential short circuit in the Printed Circuit Board Assembly (PCBA) in PoInt EVR (Power Invertor). If a short circuit occurs, it will cause the fuses to trip and the system will become non-functional due to power loss, resulting in a potential delay of procedure or termination of procedure.

FDAFeb 6, 2024Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

SPII Lubinus Prosthesis (Waldemar Link) – Labeling Confusion (2024)

Due to two complaints, has come to our attention that additional guidance is required on the correct interpretation of the carton label Size and Type columns to avoid misinterpretation during surgery.

FDAFeb 6, 2024Nationwide• Waldemar Link GmbH & Co. KG (Mfg Site) Oststr. 4-10 Norderstedt Germany

Cerebase DA Guide Sheath (Medos) – Fracture Risk (2024)

Medos has received an increase in complaints for CEREBASE DA Guide Sheath with reports of fractures at the distal end, which may result in surgical procedural delay, vascular injury and in extreme rare occasions it may result in embolism.

FDAFeb 2, 2024Nationwide• Medos International Sarl Chemin Blanc 36 Le Locle Switzerland

TING Tolnaftate Spray (Insight) – Benzene Contamination (2024)

Chemical Contamination; presence of benzene.

Class IHigh

FDAFeb 1, 2024Nationwide• Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company

Microalbumin Calibrator (Randox) – Result Misclassification (2024)

Microalbumin Calibrator Series, MA1567 & MA2426, is running with a negative bias compared to other methods and may misclassify patient results. Users may experience a shift in Quality Control and patient sample recovery of up to +12%.

FDAJan 31, 2024Nationwide• Randox Laboratories Ltd. 55 Diamond Road Crumlin (North) Ireland