stop use immediately Recalls

B Braun Medical PERIFIX FX Epidural Tray Recalled for Lid Misalignment in 48,110 Units (2025)

Potential for the lid of the catheter connector to be in the incorrect position.

B Braun Medical PERIFIX FX Epidural Tray Recalled for 0 Units in 2025

Potential for the lid of the catheter connector to be in the incorrect position.

HeartSine Pad-Pak Defibrillator Pads Recalled for 1,291,165 Units in 2025

Due to customer complaints, defibrillator pads may contain damage pins that disrupt the mechanical fit and electrical contact.

GE Medical Systems LOGIQ P10 Ultrasound Systems Recalled for 65 Units in 2025 Over UGAP Data Errors

The Ultrasound-Guided Attenuation Parameter (UGAP) measurement data may display inaccurate values representing liver steatosis. This could potentially lead to inappropriate clinical decisions impacting overall care.

GE Medical Systems LOGIQ P10 Ultrasound System Recalled for UGAP Data Inaccuracy (31 Units, 2025)

The Ultrasound-Guided Attenuation Parameter (UGAP) measurement data may display inaccurate values representing liver steatosis. This could potentially lead to inappropriate clinical decisions impacting overall care.

Goyal Group SILVER HORSE Aluminum Milk Pan & Mathar Kadaï Recalled for Lead Contamination (293 Sets,

Contains elevated levels of lead

GE Medical Systems LOGIQ P9 R4.5 Ultrasound System Recalled for Inaccurate Liver Readings (37 Units)

The Ultrasound-Guided Attenuation Parameter (UGAP) measurement data may display inaccurate values representing liver steatosis. This could potentially lead to inappropriate clinical decisions impacting overall care.

Kirkland Signature Ahi Tuna Wasabi Poke Recalled Over Listeria Risk

Listeria monocytogenes. Recall was initiated after being notified by green onion supplier of a Listeria monocytogenes positive test result in the green onions which were used only in Ahi Tuna Wasabi Poke.

Taproom Gourmet Bulk Fifth Avenue Mix Recalled for No Ingredient Label and Allergens

No ingredient label. Product contains undeclared allergens (peanuts, almonds, cashew, and soy)

Cardinal Health 200 Salem Sump Gastroduodenal Tubes Recalled Worldwide for ARV Breakage

Firm has received complaints regarding Anti-Reflux Valve (ARV) breakage due to excessive force during use. Firm is providing additional guidance for use. Expansion of RES 95214.

B. Braun Medical Recalls 5,770 PERIFIX FX Epidural Anesthesia Trays for Lid Position Issue

Potential for the lid of the catheter connector to be in the incorrect position.

Fisher & Paykel Recall 51,144 Airvo 2 and myAirvo 2 Humidifiers Over Power-Disconnect Audible Alert

Glenmark Azelaic Acid Gel Recall Affects 13,824 Tubes Sold Nationwide in 2025

CGMP Deviations: Market complaints received for gritty texture (grainy)

Percussionaire IPV In-Line Valve Recall Aims to Stop Use Over Leakage Risk in Ventilators

Baxter Healthcare Oral Probe Recalled for 5,209 Units Misconfigured as Rectal Probes (2025)

Affected oral/axillary probes were inadvertently programmed with the rectal probe configuration. Affected probes will potentially display a lower temperature than the true value, which may lead to a delay in managing fever-related symptoms or infection.

Lipton Green Tea Citrus Recalled for Undeclared Sugar in 2,854 Cases (2025)

Undeclared sugar in finished product-primary package does not reflect the product inside bottle.

Haifa Cold Smoked Sea Bass 8 oz Recalled for Listeria Contamination (2025)

D & M Smoked Fish Recalls 2,022 Haifa Cold Smoked Salmon 8 oz for Listeria Contamination (2025)

Enterix InSure ONE FIT Recall Affects 201,426 Tests Over False Negatives (2025)

InSure ONE failed sensitivity testing when used with Test Card Lot T241102, which may result in false negative results.

Park Avenue Compounding Phenylephrine HCI Syringes Recalled Over CGMP Violations