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Applied Medical Resources Corp 22872 Avenida Empresa Rancho Santa

Applied Medical Resources Corp 22872 Avenida Empresa Rancho Santa Recalls

All product recalls associated with Applied Medical Resources Corp 22872 Avenida Empresa Rancho Santa.

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Recall Summary

Total Recalls

1000

Past Year

893

Class I (Serious)

124

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 15401–15420 of 17593 recalls

Applied Medical Resources Corp 22872 Avenida Empresa Rancho Santa: Applied Medical, Lap Banding Kit, REF: K0398 Contains: ...

Potential inability to insufflate through the stopcock. Under certain circumstances, a flexible elastomeric component inside the 15mm trocar can stretch into a configuration that blocks the flow of insufflation gas (C02).

FDAJun 25, 2008Nationwide• Applied Medical Resources Corp 22872 Avenida Empresa Rancho Santa

Applied Medical Resources Corp 22872 Avenida Empresa Rancho Santa: Applied Medical, Lap Roux-EN-Y Kit, REF: K2129 Contains...

FDAJun 25, 2008Nationwide• Applied Medical Resources Corp 22872 Avenida Empresa Rancho Santa

Gyrus ACMI Corporation: Gyrus ACMI 10 Fr. Dual Lumen Catheter Reference Number: 6...

1...769 770771772 773...880

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Particulate matter in the catheter

FDAJun 25, 2008Nationwide• Gyrus ACMI Corporation

CAS Medical Systems, Inc.: 740 Series Multiparameter Monitor Software Version 3.0 Mo...

Software: Audible alarm may be silenced if changed from the factory setting

FDAJun 24, 2008Nationwide• CAS Medical Systems, Inc.

Playground Tire Swings (Miracle Recreation) – fall hazard (2008)

The recalled Tire Swing consists of a tire, which hangs from a swivel and three chains. The recall includes the following products and model numbers: Kids' Choice Arch Tire Swing Sets Model # 714-852 Kids' Choice Arch Tire Swing Extension Model # 714-852-X Kids' Choice Arch Tire Swing Swivel Replacement Model #278

CPSCJun 24, 2008Nationwide• Miracle Recreation Equipment Co., of Monett, Mo.

Philips And Neusoft Medical Systems Co., Ltd.: NeuViz Dual series computed Tomography Scanner System, X-...

Potential for R-host box and components inside to be detached of its mounting during the gantry rotor rotation. There is a potential for components to be damaged inside the system gantry and for the internal components to be expelled from the system gantry and injure the patient, operator, bystander or service people.

FDAJun 23, 2008CO, FL, IN +5 more• Philips And Neusoft Medical Systems Co., Ltd.

StatSpin, Inc., dba Iris Sample Processing: StatSampler 200 uL, Li Heparin (micro blood collector) Re...

EDTA inadvertently mixed with lithium heparin solution contained in capillary tubes.

FDAJun 20, 2008CA, CO, FL +7 more• StatSpin, Inc., dba Iris Sample Processing

Orthosoft, Inc. dba Zimmer CAS: Navitrack System - OS Knee Universal, Orthopedic Stereota...

ZIMMER CAS voluntarily conducted a retrospective recall of the Navitrack System - OS Knee Universal, due to software anomalies which were corrected with a new revision in version 2.2.1.3.

FDAJun 20, 2008CA, FL, GA +17 more• Orthosoft, Inc. dba Zimmer CAS

Orthosoft, Inc. dba Zimmer CAS: Navitrack¿ System - OS Knee Universal, Orthopedic Stereot...

ZIMMER CAS voluntarily conducted a retrospective recall of the Navitrack System - OS Knee Universal, due to software anomalies which were corrected with a new revision in version 2.2.1.3.

Class IIILow

FDAJun 20, 2008CA, FL, GA +17 more• Orthosoft, Inc. dba Zimmer CAS

Naviscan PET Systems: Naviscan PET Systems, Inc ("Naviscan") PEM Flex Solo II P...

This field correction is being initiated as a result of the firm's investigation into a report from a user indicating that the motorized compression exceeded 25 pounds of compression force during the pre-scan positioning of the patient. The investigation identified that a secondary fault protection did not perform as expected.

FDAJun 19, 2008Nationwide• Naviscan PET Systems

Civco Medical Instruments Inc: Isoloc Software, Version 6.6, 6.5 and 6.0. Part Number M...

A localization may be produced which has the incorrect moves, and therefore, could place the patient in the incorrect location.

FDAJun 18, 2008PR• Civco Medical Instruments Inc

Bush Hog Off-Road Utility Vehicles (Bush Hog) – speed control loss (2008)

The recall includes the Bush Hog Models TH440 (Trail Hunter), TH4200 (Trail Hand) and TH4400 (Trail Hand) Off-Road Utility Vehicles. "Bush Hog" is printed on the utility vehicle's cargo bed tail gate and on each side of the cargo bed. Model "TH440," "TH4200," or "TH4400" is printed on each side of the hood. The hood color is red, green, or mossy oak.

CPSCJun 18, 2008Nationwide• Bush Hog LLC, of Selma, Ala.

GE Medical Systems, LLC: GE Innova 3100 / 3100 IQ Cardiovascular Imaging System, G...

GE Healthcare has become aware that a few customers have experienced an unusual occurrence of system lockups on Innova single plane cardiovascular X-ray imaging systems while using the image auto-archiving function. when occurring during X-Ray imaging, the acquisition fails and the user has to rest the system. To date, one patient death has been reported related to this issue.

FDAJun 17, 2008AL, AK, AZ +46 more• GE Medical Systems, LLC

GE Medical Systems, LLC: GE Innova 4100 / 4100 IQ Cardiovascular Imaging System, G...

FDAJun 17, 2008AL, AK, AZ +46 more• GE Medical Systems, LLC

GE Medical Systems, LLC: GE Innova 2100 IQ Versatile Cardiac and Vascular Imaging ...

FDAJun 17, 2008AL, AK, AZ +46 more• GE Medical Systems, LLC

Medtronic Neuromodulation: Medtronic DBS" 3389 Lead Kit for Deep brain stimulation, ...

Medtronic has received reports of DBS" leads being damaged at the proximal connector end of the lead when the lead cap is used in the implant procedure. The lead damage is the result of excessive torsion and / or tensile lading of the proximal connector end of the lead. Data also suggest that excessive torque while tightening or loosening the setscrews may twist the setscrew connector block and d

FDAJun 14, 2008AL, AZ, AR +46 more• Medtronic Neuromodulation

Medtronic Neuromodulation: Medtronic DBS" 3387S-40 Lead Kit for Deep Brain Stimulati...

FDAJun 14, 2008AL, AZ, AR +46 more• Medtronic Neuromodulation

Medtronic Neuromodulation: Medtronic DBS" 3389S-40 Lead Kit for Deep Brain Stimulati...

FDAJun 14, 2008AL, AZ, AR +46 more• Medtronic Neuromodulation

Medtronic Neuromodulation: Medtronic DBS" 3387 Lead Kit for Deep brain stimulation, ...

FDAJun 14, 2008AL, AZ, AR +46 more• Medtronic Neuromodulation

Bosch Hammer Drills (Robert Bosch) – injury risk (2008)

The recalled hammer drill is blue with "BOSCH" printed on the side. The model number 1191VSR can be located on the product nameplate mounted on the side of the motor. The product's packaging will be marked as 1191VSRK (the "K" indicates that the hammer drill was packaged with a case in a kit). Only drills with a serial number that begins with "7" are included in the recall.

CPSCJun 12, 2008Nationwide• Robert Bosch Tool Corp., of Mount Prospect, Ill.