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Medtronic Perfusion Systems

Medtronic Perfusion Systems Recalls

All product recalls associated with Medtronic Perfusion Systems.

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Recall Summary

Total Recalls

1000

Past Year

620

Class I (Serious)

Most Recent

Dec 2025

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 641–660 of 10937 recalls

DLP Pediatric Arterial Cannulae (Medtronic) – Incorrect Labeling (2024)

Incorrect labeling for seven manufactured lots of certain models of Arterial Cannulae.

Low

FDADec 12, 2024Nationwide• Medtronic Perfusion Systems

Neo-Tee T-Piece Resuscitator (Mercury Medical) – Flow Controller Defect (2024)

Gas powered emergency resuscitator has a circuit flow controller manufactured with an undersized spring, which may cause resuscitator not reach the high and low ends of the PIP and PEEP pressure ranges, which may cause a loss of positive pressure, impacting effective ventilation of the patient.

Moderate

FDADec 10, 2024Nationwide• Mercury Enterprises, Inc. dba Mercury Medical

Idylla Instrument (Biocartis) – False-Positive MSI-H Results (2024)

False-positive MSI-H results generated by the Idylla MSI Test.

Moderate

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FDADec 10, 2024AL, CA, NJ +2 more• Biocartis Nv B 3 Generaal De Wittelaan 11 Mechelen Belgium

JMC5A Oxygen Concentrator (Jiangsu Jumao) – Fire Hazard Risk (2024)

Fire/Burn Risk

Oxygen concentrator may melt or catch on fire during use.

High

FDADec 9, 2024OH• JIANGSU JUMAO X-CARE MEDICAL EQUIPMENT CO LTD No

Bloody Mary Mix (Borsari) – undeclared fish and soy (2024)

Undeclared Allergen

Product contains undeclared fish (anchovy) and soy.

Class IIModerate

FDADec 9, 2024AL, AZ, CA +22 more• Borsari Food Company Inc

Portrait Core Services (GE Medical) – Patient Monitoring Software Failure (2024)

There is a software issue that can result in the loss of patient monitoring on the Portrait Central Viewer Application after 425 days of continuous run-time.

FDADec 6, 2024Nationwide• GE Medical Systems, LLC

VACATION Scented Candles (Vacation) – Fire Hazard (2024)

Fire/Burn Risk

This recall involves "The Legendary 'VACATION'" by Vacation Black Label Scented Candles. The product comes in a black glass vessel with an off-white colored fragranced wax. The product is approximately 3.75 inches in diameter by 3.5 inches tall and weighs about one pound. A foil gold color label on the candle states "The Legendary 'VACATION'" by Vacation.

CPSCDec 5, 2024Nationwide• Vacation Inc., of Miami

LINK MP Reconstruction System (Waldemar Link) – Incorrect Label Size (2024)

Error on the main label and the patient label. The labels indicate a size XXL, this is a standard-size neck segment.. All further information on the labels is correct (Length, CCD and Offset).

FDADec 5, 2024Nationwide• Waldemar Link GmbH & Co. KG (Mfg Site) Oststr. 4-10 Norderstedt Germany

Ranger ROVs (Polaris) – Vehicle Safety Issue (2024)

This recall involves certain VINs of Model Year 2024 Ranger 1000 / Crew 1000, Ranger XP 1000 / Crew XP 1000 and Ranger XP Kinetic ROVs; and ProXD Full Size/Full Size Crew and Bobcat UV34/UV34 XL UTVs. The Ranger vehicles were sold in blue, bronze, camouflage, gray, green, tan and white and in three and six seat configurations. The ProXD vehicles have gray plastic body panels with black frame/accents. The Bobcat vehicles have black side panels with white and orange accents. All UTVs have two or four seats. The Ranger and ProXD vehicles have "POLARIS" stamped on the front grille and the Bobcat vehicles have the Bobcat logo on the front grille. The Vehicle Identification Number (VIN) for the Ranger, ProXD and Bobcat vehicles is located on a portion of the left rear frame on the driver's side of the vehicle, under the cargo box.

CPSCDec 5, 2024Nationwide• Polaris Industries Inc., of Medina, Minnesota

Salmonella

Potential Salmonella

Class IHigh

FDANov 29, 2024CO• GBC Food Services, LLC dba Yummi Sushi