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Medical Components, Inc dba MedComp

Medical Components, Inc dba MedComp Recalls

All product recalls associated with Medical Components, Inc dba MedComp.

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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 23841–23860 of 25000 recalls

Medical Components, Inc dba MedComp: Jet Medical 4F x 60cm Single Lumen Polyurethane PICC Nurs...

The product is labelled as containing a 4F catheter when the trays/kits actually contain a 5F catheter. The catheters will not fit into the sheath-dilator that was included in the tray. mislabeled as 4F

FDASep 15, 2005IN, MO, OH• Medical Components, Inc dba MedComp

Bottle Sippers Pull-Up Caps (Bradshaw) – Potential Safety Issue (2005)

Choking Hazard

The recalled bottle sippers have white screw-on bases with dark blue, green or red pull-up valves. They are sold in packages of three. The package is labeled "Bottle Sippers." Bradshaw International Inc. and #70118 are written on the back of the package.

CPSCSep 15, 2005Nationwide• Bradshaw International Inc., of Rancho Cucamonga, Calif.

Medical Components, Inc dba MedComp: Jet Medical 4F Single Lumen PICC Kit. Catalog number JP7-4

1...1191 119211931194 1195...1250

Page 1193 of 1250Next

FDASep 15, 2005IN, MO, OH• Medical Components, Inc dba MedComp

VIASYS Med Systems: Stackhouse Lens/Hood, Mark III Universal; a sterile dispo...

The packaging may be compromised such that sterility of the hoods cannot be guaranteed.

FDASep 13, 2005Nationwide• VIASYS Med Systems

Accumetrics Inc: Accumetrics part number 29001 VerifyNow Instrument, print...

In 2001, separate reports of mild shock, sparking and smoke from Accumetrics PN 29001 power supply.

FDASep 13, 2005CA, FL, IL +6 more• Accumetrics Inc

VIASYS Med Systems: Stackhouse FreedomAire Lens/Hood; a sterile disposable pr...

The packaging may be compromised such that sterility of the hoods cannot be guaranteed.

FDASep 13, 2005Nationwide• VIASYS Med Systems

Terumo Cardiovascular Systems Corp: Terumo Sarns brand Flexible arterial cannula, 7.5 mm (22 ...

There may be a solvent bond failure at the tubing/connector site of the cannula, resulting in the disconnection of the cannula parts.

FDASep 12, 2005Nationwide• Terumo Cardiovascular Systems Corp

Avid Medical Inc: Custom Procedure Trays, containing various configurations...

Defect in packaging of medical devices may compromise sterility of these products used in medical and surgical procedures.

FDASep 9, 2005Nationwide• Avid Medical Inc

Gas Grills and Patio Heaters (Coleman) – Safety Concerns (2005)

Fire/Burn Risk

The recall includes Coleman® Gas Grills with model numbers 5100, 5300, 5400, 5600, 6000 and 7700, and Coleman® Patio Heater with model number 5040. The model name and number can be found directly on the front of the grills and on the inside cover of the heaters.

CPSCSep 8, 2005Nationwide• The Coleman Company, Inc., of Wichita, Kan.

Golf Cars (E-Z-GO) – Vehicle Performance Issue (2005)

Fire/Burn Risk

The recall involves certain model year 2002 through 2005 E-Z-GO Fleet and E-Z-GO Freedom gasoline-powered golf cars and Shuttle 2+2 personnel carriers. The model names for the recalled products are TXT, Freedom and Shuttle 2+2. The model names are printed on the sides of the Freedom and Shuttle 2+2 vehicles, and the E-Z-GO logo is on the front of all three vehicles. The recalled vehicles have 9-horsepower engines and serial numbers ranging from 1451059 through 2341739. The serial numbers of early production vehicles are found on plates located on the passenger side dash housing. The serial numbers of late production vehicles are found on plates located on the body below the driver's seat and on the chassis between the seat back supports.

CPSCSep 8, 2005Nationwide• E-Z-GO, of Augusta, Ga. - A Textron Company

AGA Medical Corporation: AMPLATZER Duct Occluder, Order No. 9-PDA-003, Device Siz...

The pointed end of a screw securing the occluder to the delivery cable could scrape off microscopic fragments of the polytetrafluorethylene (PTFE) plastic lining of the sheath. Those shavings could potentially migrate into a patient's bloodstream.

FDASep 6, 2005Nationwide• AGA Medical Corporation

Merit Medical Systems, Inc: Merit Custom Procedure Kit

Component of procedure kits may allow higher than desired amount of IV solution to be infused in to patient during pressure monitoring procedure.

FDASep 2, 2005MD, OR, VA +1 more• Merit Medical Systems, Inc

Sesame Street Sunglasses (American Greetings) – Safety Risk (2005)

Choking Hazard

This recall involves DesignWare® child-size sunglasses with Sesame Street character decals. Sold in quantities of four, each package contains a yellow, blue, red and green pair of sunglasses. The bright green cardboard backer has the Sesame Street and DesignWare® logo on the front, and model number SUN-1219 on the back.

CPSCSep 1, 2005Nationwide• American Greetings Corp., of Cleveland, Ohio

B. Braun Medical, Inc.: 7F Locking Tearaway Introducers non-sterile. Part number ...

Tear away sheath assembly may contain a sheath (8FR) that is not the correct French size for the dilator (7FR).

FDASep 1, 2005Nationwide• B. Braun Medical, Inc.

Terumo Cardiovascular Systems Corp: Terumo Advanced Perfusion System 4 inch diameter Roller P...

The pump may stop during the autodose delivery without completion of the dose delivery to the patient.

FDASep 1, 2005Nationwide• Terumo Cardiovascular Systems Corp

AGA Medical Corporation: AMPLATZER Vascular Plug, Manufactured by AGA Medical Corp...

Five lots of AMPLATZER Vascular Plugs were sterilized in a load that was not validated for the AMPLATZER Vascular Plug. However, only three of those five lots were distributed.

FDASep 1, 2005Nationwide• AGA Medical Corporation

Smiths Medical PM, Inc.: Advisor Vital Signs Monitor (model 9200), catalog number ...

Potential Safety related problem associated with the pace detect function on some Advisor monitors that have impedance respiration capabilities in that random pace markers may appear when the pace detect function is turned on and the primary lead is set to Lead II, III or any of the augmented leads, AVL, AVR or AVF on the Advisor monitor.

FDASep 1, 2005AZ, CA, KS +4 more• Smiths Medical PM, Inc.

Enpath Medical, Inc.: Enpath Steerable Sheath, model 10775-003, Sterile EO. Si...

Enpath has become aware that some of the Enpath Medical 8 Fr Steerable sheath devices may have non-conforming hemostasis valves in that the valve can leak or the valve was observed to have a small hole.

FDAAug 31, 2005MA• Enpath Medical, Inc.

Back Trails Jr. Bicycle Helmets (Target) – Safety Issue (2005)

The recall includes Target's "Back Trails Jr." brand toddler, youth and child bicycle helmets sold in various colors. They were manufactured after January 1, 2004. Helmet model numbers: 89888 or 88003 (toddler), 89951 or 88001 (girl's 8-vent youth), 89952 or 88002 (boy's 8-vent youth), or 89917 (14-vent child's) appear on a white label inside the helmets, along with date of manufacture (YYYY/MM/DD) and the words "Made in China." Target product identification numbers: 082-01-0520 (toddler), 082-01-0149 (girl's 8-vent youth), 082-01-0189 (boy's 8-vent youth), and 082-01-0334 (14-vent child's) and the brand name "back trails jr.," appear on the product packaging.

CPSCAug 31, 2005Nationwide• UNA International Limited, of China

Maptangle™ World Edition Floor Mat (Team WorldWide) – Geographic Placement Error (2005)

The floor map game consists of a 6-foot by 5.5-foot vinyl Maptangle™ floor mat that has various multicolored geographic locations and landmarks painted on the floor mat and a set of 103 playing cards, consisting of corresponding geographic locations and landmarks. The object of the game is for a team of players to locate and place their feet on all of the landmarks and geographic locations. The game is age-graded for children 7 years and up. This recall pertains only to the floor mat and does not include any other components of the game. Floor mat map games with manufacture date codes are not subject to this recall.

CPSCAug 25, 2005Nationwide• Team WorldWide Corp., of Taipei City, Taiwan (floor mat only)