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Merit Medical Systems, Inc.

Merit Medical Systems, Inc. Recalls

All product recalls associated with Merit Medical Systems, Inc..

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

127

Most Recent

Jan 2026

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 22361–22380 of 25000 recalls

Merit Medical Systems, Inc.: University Health System Custom Cardiac Cath Pack, K09T-0...

A manufacturing defect may prevent adequate sterilization of the entire device.

FDAJan 29, 2009Nationwide• Merit Medical Systems, Inc.

Merit Medical Systems, Inc.: Custom Angiographic Kit, K09-MS3084, Sterile EO, Merit Me...

A manufacturing defect may prevent adequate sterilization of the entire device.

FDAJan 29, 2009Nationwide• Merit Medical Systems, Inc.

Merit Medical Systems, Inc.: Custom Cardiac Cath Pack Kit, K09-08945, Sterile EO, Meri...

A manufacturing defect may prevent adequate sterilization of the entire device.

FDAJan 29, 2009Nationwide

1...1117 111811191120 1121...1250

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• Merit Medical Systems, Inc.

Merit Medical Systems, Inc.: Jeanes Hospital Custom Cath Procedure Tray, K09T-08945, S...

A manufacturing defect may prevent adequate sterilization of the entire device.

FDAJan 29, 2009Nationwide• Merit Medical Systems, Inc.

Philips Medical Systems (Cleveland) Inc: TumorLoc software for the Brilliance Big Bore (BB) and th...

A software error in the TumorLoc software was discovered upon receipt of a customer complaint. There is the potential for data to be lost during reconstruction of images in which slices can either be discarded, or interleaved based upon their series ID.

FDAJan 28, 2009Nationwide• Philips Medical Systems (Cleveland) Inc

LCD Television Wall Mounts (Milestone AV) – Cracking Risk (2009)

These wall mounts are used with flat screen LCD televisions. The recalled wall mounts are INIT models NT-TVM103 and NT-TVM104. The model numbers can be found on the UL sticker on the television interface.

CPSCJan 27, 2009Nationwide• Milestone AV Technologies, of Savage, Minn.

Glider Recliners (Lane) – Fall Hazard (2009)

The recall involves Lane's Glider Recliners, model numbers 2056 and 2085. Affected recliners have a manufacture date between June 2008 and October 2008. The model number, manufacture date and 9-digit serial number can be located beneath the footrest of the recliner.

CPSCJan 27, 2009Nationwide• Lane Furniture Industries Inc., of Tupelo, Miss.

Varian Medical Systems Oncology Systems: Varian Medical Systems Floorstand. An accessory of the Op...

Potential patient impact -- limit switches for Floorstand may be inadequate for some models and allow for potential impact.

FDAJan 26, 2009FL, IN, WI• Varian Medical Systems Oncology Systems

Philips Medical Systems (Cleveland) Inc: GEMINI PET/CT Systems Upper Patient Pallet for the GEMINI...

Upper patient pallet component of the recalling firm's Gemini PET/CT system may be thinner than normally required, which may reduce the product's load bearing capacity, resulting in cracking under less than the designed full-load weight.

FDAJan 26, 2009CA, GA, IN +2 more• Philips Medical Systems (Cleveland) Inc

Phillips Nuclear Medicine: Precedence SPECT/CT System, Precedence 16 3/8, Upper Pati...

A problem has been identified with some upper patient pallets on Precedence SPECT/CT System, which may reduce its load bearing capacity and may result in its cracking. If this were to happens, could pose a risk to patient.

FDAJan 26, 2009Nationwide• Phillips Nuclear Medicine

Stationary Bicycle Trainers (Saris) – Fall Risk (2009)

The recalled trainers are a stationary frame that allows bicycles to be converted into stationary bicycles. The recalled models include: CycleOps Pro Series Trainer models 9014 (SuperMagneto Pro), 9331 (JetFluid Pro), 9460 (PowerBeam Pro), 9321 (JetFluid Pro Winter Training Kit), and 9322 (SuperMagneto Pro Winter Training Kit) without the secondary locking pin. The model number and style names are printed on the left side of the main frame of the trainer.

CPSCJan 22, 2009Nationwide• Saris Cycling Group, of Madison, Wis.

Rheem Oil-Fired Furnaces (Rheem) – Fire Hazard (2009)

Fire/Burn Risk

This recall involves oil-fired furnaces sold under the Rheem, Ruud and United Refrigeration brands. Only the models beginning with the model numbers listed in the chart below and with date codes ending in 0106 through 5206, 0107 through 5207, or 0108 through 4808 are included in this recall. The model number and date code (designated by the four digits following an "M" in the middle of the serial number) are printed on the unit's rating plate, which is on the left wall of the furnace's interior just above the burner. The rating plate can be found by opening the unit's burner access door, which has slotted openings. Model # Brand & Description ROBF Rheem Classic/Ruud Achiever High Efficiency Upflow Oil Furnace ROPF Rheem Classic/Ruud Achiever High Efficiency Downflow/Horizontal Oil Furnace TZOUP United Refrigeration "Thermal Zone" Upflow Oil Furnace TZODH United Refrigeration "Thermal Zone" Downflow/ Horizontal Oil Furnace

CPSCJan 22, 2009Nationwide• Air Conditioning Division of Rheem Manufacturing Co., of Fort Smith, Ark.

Philips Medical Systems North America Co. Phillips: Product's marketing brochure is labeled in part: "Philips...

Patient and image data can be exchanged when a patient is selected in the patient list and the examination tab is pressed with background query running at the same time. There is a risk that the data may then be linked to the incorrect patient, which may adversely affect diagnosis and treatment.

FDAJan 21, 2009AL, AK, AZ +42 more• Philips Medical Systems North America Co. Phillips

Draeger Medical, Inc.: Carina Home Ventilator. The device is used as a continuo...

The device may not generate a pilot line disconnect alarm if the pilot line becomes disconnected, which may potentially result in a substantial reduction in tidal volume delivery.

FDAJan 21, 2009Nationwide• Draeger Medical, Inc.

Computerized Medical Systems Inc: Focal Radiation Treatment Planning System, Focal Release...

Focal: the couch position can be moved between scans of the same CT study. When the images are imported into Focal, the software is not checking the DICOM Image Position (Patient) tag and therefore is not aligning the images sets if there are different couch positions indicated. A shift between image sets will exist of the same amount that the CT couch was moved.

FDAJan 19, 2009Nationwide• Computerized Medical Systems Inc

Rainforest Portable Play Yards (Simplicity) – Fall Risk (2009)

The recalled play yards are portable and were sold with a bassinet, changing table, and mobile features. The products have a Rainforest™ patterned fabric, Rainforest themed artwork and bear the "Fisher-Price" logo. The Simplicity Inc. model numbers are 5310 RNF, 5310RNFC, 5310RNFT and 5310RNFW. The model number is located on a sticker on one of the legs underneath the play yard.

CPSCJan 15, 2009Nationwide• Simplicity Inc., of Reading, Pa. (The firm is out of business)

Lexamed: BEC Growth Chek Microbial Suspension - Candida albicans C...

Candida albicans microbial suspension, certified to deliver less than 100 organisms per dose, was found to have a population count which exceeded 100 organisms per dose, following distribution.

FDAJan 13, 2009UT• Lexamed

Newport Medical Instruments Inc: Newport HT50 Ventilator. Model #HT50 H1-B The device ...

The recall was initiated because Newport Medical Instruments confirmed that the Newport HT50 ventilators that were shipped in December 2008 were without the label on the top of the ventilator that reminds users to keep HT50 ventilators plugged into an external power supply whenever possible to preserve the longterm capacity of the battery.

FDAJan 13, 2009OH, VA, WA +1 more• Newport Medical Instruments Inc

Stork Craft Baby Cribs (Stork Craft) – Entrapment Risk (2009)

This recall involves Stork Craft Baby cribs and Stork Craft cribs with the Fisher-Price logo. All Stork Craft Baby cribs with manufacturing and distribution dates between May 2000 and November 2008 are included in this recall. All Stork Craft cribs with the Fisher-Price logo have distribution dates between May 2000 and December 2004. The cribs were sold in various styles and finishes. The manufacture date, model number, crib name, country of origin, and the firm's name, address, and contact information are located on the assembly instruction sheet attached to the mattress support board. The firm's insignia "Storkcraft baby" or "storkling" is inscribed on the drop side teething rail of some cribs. In the product that contains the "Fisher-Price" logo, this logo can be found on the crib's teething rail, in the manufacturer's instructions, on the assembly instruction sheet attached to the mattress support board, and on the end panels of the Twinkle-Twinkle and Crystal crib models.

CPSCJan 13, 2009Nationwide• Stork Craft Manufacturing Inc., of British Columbia, Canada

Terumo Cardiovascular Systems Corporation: Terumo Advanced Perfusion System 1 Central Control Monito...

The monitor may exhibit start-up failure, video/display issues, calibration issues, and partial or complete loss of functionality during use.

FDAJan 12, 2009Nationwide• Terumo Cardiovascular Systems Corporation