Food & Beverages
HIGH
FDA FOOD
CNC Noodle Corp Fresh Noodles Recalled for Undeclared Wheat and Yellow Dye 6 (Tartrazine) in 310-Box
CNC Noodle
Undeclared wheat
Recall database
All Product Recalls
Browse 4,434 active product recalls and safety alerts. Use search and filters to narrow the list by product, brand, hazard level, or status.
- Active recalls
- 4,434
- Current page
- 79
Health & Personal Care
CRITICAL
FDA DEVICE
Philips Respironics Trilogy Evo O2 Ventilator Recall Covers 113,717 Units Worldwide (2026)
Using non-pneumatic nebulizers with Trilogy Evo Platform ventilators may result in a discrepancy between the set tidal volume and the tidal volume received by the patient.
Philips Respironics
Using non-pneumatic
Health & Personal Care
HIGH
FDA DEVICE
Philips Respironics Trilogy Evo Ventilators Recalled for Tidal-Volume Mismatch (113,717 Units, 2026)
Using non-pneumatic nebulizers with Trilogy Evo Platform ventilators may result in a discrepancy between the set tidal volume and the tidal volume received by the patient.
Philips Respironics
Using non-pneumatic
Health & Personal Care
HIGH
FDA DEVICE
Civco Medical Instruments Recalls 10 eTRAX Needle Sensor 16G for Aurora Trackers (2026)
There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.
Civco Medical Instruments
There was
Health & Personal Care
HIGH
FDA DEVICE
Civco Medical Instruments Recalls 21 eTRAX Needle Sensors for Aurora Trackers (2026)
There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.
Civco Medical Instruments Co.
There was
Health & Personal Care
CRITICAL
FDA DEVICE
Philips Respironics Trilogy Evo O2 Ventilator Recall Affects 113,717 Units in 2026
In some situations, the Obstruction Alarm does not trigger within the timeframe dictated by the relevant standards and may take up to four breaths.
Philips Respironics
In some
Health & Personal Care
HIGH
FDA DEVICE
Philips Respironics Trilogy Evo Ventilator Recall 2026 Affects 113,717 Units
In some situations, the Obstruction Alarm does not trigger within the timeframe dictated by the relevant standards and may take up to four breaths.
Philips Respironics
In some
Food & Beverages
HIGH
FDA FOOD
CNC Noodle Recall: 427 Cases of Steam Noodles Recalled for Undeclared Wheat (2026)
CNC Noodle
Undeclared wheat.
Health & Personal Care
HIGH
FDA DEVICE
Philips Respironics Trilogy Evo Universal Ventilator Recall 113,717 Units (2026)
In some situations, the Obstruction Alarm does not trigger within the timeframe dictated by the relevant standards and may take up to four breaths.
Philips Respironics
In some
Health & Personal Care
HIGH
FDA DEVICE
Civco Medical Instruments Recalls 6 eTRAX Needle System Starter Kits for Aurora Trackers (2026)
There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.
Civco Medical Instruments Co.
There was
Health & Personal Care
HIGH
FDA DEVICE
Philips Respironics Trilogy EV300 Recalled 113,717 Units Worldwide for Tidal Volume Discrepancy (202
Using non-pneumatic nebulizers with Trilogy Evo Platform ventilators may result in a discrepancy between the set tidal volume and the tidal volume received by the patient.
Philips Respironics
Using non-pneumatic
Health & Personal Care
HIGH
FDA DEVICE
Civco Medical eTRAX 14G Needle Sensor Recall for 5 Units (2026)
There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.
Civco Medical Instruments Co.
There was
Health & Personal Care
HIGH
FDA DEVICE
Civco Medical Instruments Recalls 2 eTRAX 12G Starter Kits for Aurora Trackers (2026)
There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.
Civco Medical Instruments
There was
Health & Personal Care
HIGH
FDA DEVICE
Philips Respironics Trilogy EV300 Ventilator Recall Affects 113,717 Units in 2026
In some situations, the Obstruction Alarm does not trigger within the timeframe dictated by the relevant standards and may take up to four breaths.
Philips Respironics
In some
Health & Personal Care
HIGH
FDA DEVICE
Civco Medical Instruments Recalls 20 eTRAX Needle System Starter Kit 18G for Aurora Trackers (2026)
There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.
Civco Medical Instruments
There was
Health & Personal Care
HIGH
FDA DEVICE
Civco Medical Instruments eTRAX Needle System Starter Kit 16G Recall for 18 Units (2026)
There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.
Civco Medical Instruments Co.
There was
Health & Personal Care
LOW
FDA DEVICE
Civco Medical Instruments Recalls 5 eTRAX Needle Sensor 12G for Aurora Trackers (2026)
There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.
Civco Medical Instruments
There was
Health & Personal Care
CRITICAL
FDA DEVICE
Philips Respironics Trilogy Evo Universal Ventilator Recall Affects 113,717 Units Worldwide in 2026
Using non-pneumatic nebulizers with Trilogy Evo Platform ventilators may result in a discrepancy between the set tidal volume and the tidal volume received by the patient.
Philips Respironics
Using non-pneumatic
Health & Personal Care
HIGH
FDA DEVICE
Medline NAMIC Angiographic Rotating Adaptor Syringes Recalled in 2,980 Kits Worldwide
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
Medline Industries, LP
Medline Industries,
HIGH
FDA DEVICE
Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes EXTREMITY PACK DYNJ34846C HAND PACK DYNJ83218A, DYNJ85396 LAMINECTOMY DYNJ905156R MAJOR...
Unapproved design changes to the products outside of the 510(k) clearance.
Medline Industries, LP
Unapproved design