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Ossur H F Grjothals 5 Reykjavik Iceland

Ossur H F Grjothals 5 Reykjavik Iceland Recalls

All product recalls associated with Ossur H F Grjothals 5 Reykjavik Iceland.

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Recall Summary

Total Recalls

1000

Past Year

593

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 1221–1240 of 10391 recalls

Power Knee (Ossur) – battery failure risk (2023)

Knee batteries may need replacement with conforming batteries to ensure there isn't a failure to turn on the device, or an unexpected shutdown, which is a momentary loss of power to the knee where the user may experience loss of support that can lead to a fall and potential injury.

FDADec 26, 2023Nationwide• Ossur H F Grjothals 5 Reykjavik Iceland

Benzonatate Capsules (Amerisource) – Superpotent Drug (2023)

Superpotent drug: Assay results were slightly above specification at the time zero point.

Class IIILow

FDADec 26, 2023Nationwide• Amerisource Health Services LLC

Robitussin Honey CF Max Non-Drowsy (Haleon) – Microbial Contamination (2023)

Microbial Contamination of Non-Sterile Products

Class I

1...60 616263 64...520

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High

FDADec 26, 2023Nationwide• Haleon US Holdings LLC

Robitussin Honey CF Max Nighttime (Haleon) – Microbial Contamination (2023)

Microbial Contamination of Non-Sterile Products

Class IHigh

FDADec 26, 2023Nationwide• Haleon US Holdings LLC

Baxter Exactamix Pro (Baxter) – overfill software error (2023)

An error was identified in software versions 2.0.8 and 2.1.8 while using the "Use Some Overfill" feature which may lead to over-delivery of an ingredient. This issue can result in redundant ingredient delivery of the requested overfill volume.

FDADec 22, 2023AL, AZ, CA +19 more• Baxter Healthcare Corporation

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

Solgar Glucosamine Chondroitin (Nestle) – packaging error (2023)

Nestle Health Science has initiated a recall of Solgar Glucosamine Chondroitin, 120 Tablets, in Glass bottle, 12 bottles per case because of error during packaging in which a A Megasorb B-Complex product was filled into bottles labeled as Glucosamine_Chondroitin MSM.

Class IIILow

FDADec 22, 2023IN, NV, NY +3 more• Nestle Product Technology Center - Nestle Health Science

Baxter Exactamix Pro (Baxter) – overfill software error (2023)

FDADec 22, 2023AL, AZ, CA +19 more• Baxter Healthcare Corporation

Cardinal Health Suction Canister (Cardinal Health) – suction loss risk (2023)

The above-listed lots of Cardinal Health Medi-Vac CRD" Suction Canister Liners 1L may experience loss of suction on low or low intermittent suction settings, due to a misalignment of the liner with the outer hard canister.

FDADec 21, 2023Nationwide• Cardinal Health 200, LLC

Cardinal Health Suction Canister (Cardinal Health) – suction loss risk (2023)

FDADec 21, 2023Nationwide• Cardinal Health 200, LLC

Cardinal Health Suction Canister (Cardinal Health) – suction loss risk (2023)

FDADec 21, 2023Nationwide• Cardinal Health 200, LLC

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

BrightView XCT Gamma Camera (Philips) – Detector Fall Risk (2023)

Laceration Risk

Detector may unexpectedly fall due to a component failure. If the detector is positioned below center of gantry, there is a potential for abrasion, contusion, laceration, and/or fracture to the patient's lower limbs, as well as an interruption to normal system operation. If detector is positioned above center of gantry, there may be an interruption to normal system operation.

FDADec 15, 2023Nationwide• Philips North America

ProxiDiagnost N90 (Philips) – Mixed Patient Images (2023)

Issue 1: Mixed Images: The Radio Fluoroscopy (RF) viewer may also display a previous patient s radiography (RAD) images when starting the next patient scan while the previous patient image export is still processing. If the issue occurs, there is a potential for incorrect patient data to be displayed in the image. Issue 2: Detector Access point: Security vulnerability specific to the Wireless Portable Detector configuration items in Philips Support Connect (PSC). Due to this vulnerability it is possible, with physical access to the system and knowledge of specific settings, to modify and export data to removable media (example: USB)

FDADec 15, 2023Nationwide• Philips North America

ProxiDiagnost Upgrade (Philips) – Mixed Patient Images (2023)

Issue 1: Mixed Images: The Radio Fluoroscopy (RF) viewer may also display a previous patients radiography (RAD) images when starting the next patient scan while the previous patient image export is still processing. If the issue occurs, there is a potential for incorrect patient data to be displayed in the image. Issue 2: Detector Access point: Security vulnerability specific to the Wireless Portable Detector configuration items in Philips Support Connect (PSC). Due to this vulnerability it is possible, with physical access to the system and knowledge of specific settings, to modify and export data to removable media (example: USB)

FDADec 15, 2023Nationwide• Philips North America

BrightView Gamma Camera (Philips) – Detector Fall Risk (2023)

Laceration Risk

FDADec 15, 2023Nationwide• Philips North America

BrightView X Gamma Camera (Philips) – Detector Fall Risk (2023)

Laceration Risk

FDADec 15, 2023Nationwide• Philips North America

IgM Total Test (Siemens) – Potential Negative Bias (2023)

Potential for a negative bias with quality control (QC) and patient sample results when using the Atellica CH Immunoglobulin M_2 (IgM_2) reagent.

FDADec 15, 2023Nationwide• Siemens Healthcare Diagnostics, Inc.

Azurion System (Philips) – Imaging Functionality Loss (2023)

System may exhibit a loss of imaging functionality and data due to an issue which can cause the system to continuously restart. If the issue occurs during a procedure, there may be a delay and/or abortion of the procedure.

FDADec 12, 2023Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

TECNIS Toric II IOL (Johnson & Johnson) – Angle Specification Issue (2023)

Due to intraocular lens containing an angle out of specification (OOS). The cylinder axis marks do not meet product specifications for the allowable angle between Low Power Meridian (LPM) and toric cylinder axis marks.

FDADec 12, 2023Nationwide• Johnson & Johnson Surgical Vision, Inc.