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Other Medical Devices

🏥 Medical Devices • 15,809 recalls

Intera 1.5T

Philips North America

Class I - Dangerous

Potential component failure in the Gradient Coil could product smoke and/or fire.

Oct 23, 2023 Other Medical Devices Nationwide View Details →

Alinity c Iron Reagent, Reference Number 08P3920

Sentinel CH SpA

Class I - Dangerous

A high recovery of Iron assay has been observed at some customer sites. Internal studies confirmed the positive shift of Quality Control and patient samples results, up to 15% for Iron Products (Alinity c Iron Reagent REF. 08P3920) to be used on Abbott Alinity Instrument and to 30% for Iron Products (IRON REF. 6K95-41 and IRON REF. 6K95- 30) to be used on Abbott Architect Instrument. When using the affected lots, there is a potential for delay in reporting patient results due to QC failure, also a potential for falsely elevated results.

Sep 29, 2023 Other Medical Devices Nationwide View Details →

GEM Premier 3000 PAK - pH, pCO2, pO2, Hct, Na+, K+, Ca++, Glucose and Lactate, Part Numbers 00024315009, 00024330009, 00024345009, 00024360009

Instrumentation Laboratory

Class I - Dangerous

Internal testing identified that the GEM Premier PAKs (cartridges) may exhibit an over-recovery (i.e., positive bias) of pO2 results in the low range (at pO2 levels less than 60 mmHg) that are outside of labeled performance specifications for pO2. The positive bias may lead to false positive for medical decision levels at pO2 < 60 mmHg, which may result in failure to detect and/or adequately treat hypoxemia and lead to a delay in treatment. The quality control procedures for the Non-iQM GEM Premier 3000 may not detect the non-conformance.

Sep 29, 2023 Other Medical Devices View Details →

Uretero-reno fiberscope-For endoscopic diagnosis and treatment within the ureter and kidney. Model Numbers: URF-P7, URF-P7R, URF-V2, URF-V2R, URF-V3, URF-V3R.

Aizu Olympus Co.

Class I - Dangerous

Channel air drying process was not validated, and that a small percentage of scopes returned to customers after repair had a wet channel. Water remaining in the channel of the endoscopes has the potential for contamination that could lead to the risk of infection

Sep 25, 2023 Other Medical Devices Nationwide View Details →

Spectral CT on Rails, Software Version 5.1.0, Model Number 728334

Philips North America

Class I - Dangerous

This recall is part of a 2-issue recall for the same system. When using the IVC needle position button, on the IVC control box during a series of scans, the plan box may not move to the desired needle position. This issue could result in the gantry moving to a location the operator does not expect. If this occurs, it presents a risk that the scan could occur at an incorrect location, or that the unintended motion of the gantry could cause a collision with the user or needle. The other part of the recall involves a software crash when the CCT foot pedal is activated (as described in RES ID93363).

Oct 9, 2023 Other Medical Devices Nationwide View Details →

Ocean Water Seal Chest Drains (Ocean): Products REF Number Product Name (1)2002-000 DRAIN, OCEAN SINGLE W/AC,S; (2)2002-040 DRAIN, OCEAN SINGLE,PEDI CONNECTOR; (3)2002-100 DRAIN, OCEAN SINGLE W/AC; (4)2002-300 DRAIN, OCEAN SINGLE W/S; (5) 2002-400 DRAIN, OCEAN SINGLE ; (6)2012-320 DRAIN, OCEAN PEDI W/S; (7)2050-000 DRAIN, OCEAN BRU W/AC,S

Atrium Medical

Class I - Dangerous

Instructions for Use (IFU) for the Atrium Ocean, Oasis, and Express chest drains do not provide sufficient precaution instruction for proper set up of catheter(s) and patient tube connections with single collection chamber chest drains

Sep 18, 2023 Other Medical Devices Nationwide View Details →

BLOOD CULTURE KIT, REF DYNDH1647B

MEDLINE INDUSTRIES, LP - Northfield

Class I - Dangerous

This recall is being issued due to items within the kit have expired prior to the overall kit expiration date listed on the insert.

Nov 1, 2023 Other Medical Devices Nationwide View Details →
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