Fish Recalls in the United States

Philips North America Llc recalls Philips Brilliance. Models: Brilliance iCT, Brilliance iCT U

Philips has identified an unintended radiation issue with the Philips IQon, iCT, Ingenuity, and Brilliance CT 64 systems that could affect the performance of the equipment.

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Philips North America Llc recalls Philips IQon Spectral CT Product Codes: IQon Spectral CT

Philips has identified an unintended radiation issue with the Philips IQon, iCT, Ingenuity, and Brilliance CT 64 systems that could affect the performance of the equipment.

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Medline Industries, LP recalls Medline Convenience Kits: 1) IV START KIT, Catalog Number:

The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in the paper lidding which may extend to the seal area. If the sterile barrier is compromised, patients and users may be exposed to microbial contamination. Potential health consequences may include no injury, localized infection, or, less commonly, more serious infection requiring medical treatment, antimicrobial therapy, procedural intervention, or hospitalization. In rare cases, particularly in critically ill or immunocompromised patients, severe infection could become life-threatening.

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Medline Industries, LP recalls Medline Convenience Kits containing BD ChloraPrep Clear - 1m

Downstream recall - manufacturer recalled specific lots of BD ChloraPrep Clear - 1mL Applicators. Affected product may exhibit an open or incomplete seal on the packaging of the applicator. Use of potentially contaminated applicator may lead to localized skin or soft tissue infection, or systemic infection or infectious complications.

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Philips North America Llc recalls Philips Ingenuity CT Product Codes: Ingenuity CT Upgrades 7

Philips has identified an unintended radiation issue with the Philips IQon, iCT, Ingenuity, and Brilliance CT 64 systems that could affect the performance of the equipment.

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Philips North America Llc recalls Philips Brilliance CT 64: Brilliance CT 64 Channel Product C

Philips has identified an unintended radiation issue with the Philips IQon, iCT, Ingenuity, and Brilliance CT 64 systems that could affect the performance of the equipment.

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Henry Schein Inc. recalls Grandio Universal Nano-Hybrid Restorative Material - Capsule

Specific lots were distributed in the US with incorrect packaging and Instructions for Use (IFU) from the U.S. FDA-cleared device.

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Philips Healthcare (Suzhou) Co., Ltd. recalls Philips Incisive CT with software V4.5&V5.0, Product Code 72

Potential of failing to trigger clinical scan during Bolus Tracking.

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Henry Schein Inc. recalls Structur 2 SC Temporary Resin Cartridge Refill 75Gm, Product

Specific lots were distributed in the US with incorrect packaging and Instructions for Use (IFU) from the U.S. FDA-cleared device.

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