electronic Recalls

Medtronic MiniMed CareLink Clinic Recall 12,126 Units Worldwide in 2025

Mindray Sevoflurane V90 Vaporizer Recalled for Leakage Risk in A9 System (148 Units)

Mindray DS USA recalled 148 Sevoflurane V90 electronic vaporizers used with the A9 Anesthesia System. The devices have a potential for anesthesia leakage. Healthcare facilities should stop using the device immediately and follow manufacturer instructions.

Mindray DS USA Recalls 54 Isoflurane V90 Vaporizers for A9 Anesthesia System Over Leakage Risk (2025

M.C.I. Foods Recalls 1,040 Cases of Ready-to-Eat Egg & Cheese Breakfast Burritos and Wraps (2025)

Cooked egg ingredient for Ready-to-Eat products tested positive for Listeria Monocytogenes

iFIT Recalls NordicTrack Rowing Machines Over Fire Hazard (NTRW19147.0–.3)

DERMASENSOR DermaSensor 10101 Diagnostic Device Recalled for 9 of 343 Units (2025)

Potential for device to not meet specifications resulting in incorrect results or delay of referral for patients.

Glycar SA Recalls 18 SJM Pericardial Patch EnCap 5x10 cm REF C0510 in 2025 Recall

The impacted lot may not meet the required tensile strength specification.

ESR HaloLock Wireless Power Banks Recalled in Expansion to Include 2G505 Model for Fire and Burn Haz

STAQ Pharma Ketamine Hydrochloride Injection 50 mL Recall for Labeling Errors (2025)

Labeling: Incorrect or Missing Lot and/or Exp Date

Almpal Dissolved Oxygen Test Kits Recalled for Non–Child-Resistant Sulfuric Acid Packaging

This recall involves Almpal dissolved oxygen test kits. The test kits come in a cream-colored box bearing a white label with "Dissolved Oxygen Test Kit" and the manufacture date, batch number, and expiration date printed on it.

Abiomed Impella Controller Recall Aims to Address Cybersecurity Vulnerabilities Across 32 Product SK

Potential cybersecurity vulnerabilities related to the operating system in the Automated Impella Controller (AIC).

Philips Medical Systems Nederland 718096 Zenition 50 Interventional X-Ray System Recalled in 2025

Over time some systems may experience loss of imaging functionality and/or poor image quality due to potential corrosion of the Image Intensifier Television (IITV) control board.

Wholesale Produce Supply LLC Recalls 307 Cases of Cut Fresh Fruit Mix Over Listeria Risk (2025)

Synthes 5.0mm IM Nail Screw Recalled for Labeling Error (2025)

Although the etched length on the screw is correct, the length marked on the external packaging is incorrect. Specifically, 42mm screws were packaged and labeled as 46mm, while 46mm screws were packaged and labeled as 42mm.

Georgia Nut Co Recalls 76,121 Cases of tru fru Creme Freeze-Dried Strawberries 3.4 oz (2025)

potential for metal in product

BD BACTEC Blood Culture System Recall 1,086 Units Worldwide Over Unauthorized Access Risk (2025)

BD Phoenix M50 Recall: 4,283 Systems Worldwide Over Access Risk (2025)

Biomet ZipTight AC Joint Implant Recall for 98 Units Over Missing Slotted Button (2025)

There is a potential for a missing slotted button assembly in one lot of ZipTight, Acute AC Joint Implant, Single Ziploop

BD Recalls 177 BACTEC Blood Culture System Units Over Unauthorized Access Risk (2025)

El Rojo Wholesale Recalls 2,904 Boxes of Pasta De Harina for Missing Ingredients and Nutrition Panel

Product is missing the ingredient list (which lead to missing wheat and Yellow No. 6), and a nutritional panel.