Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means the agency’s own highest classification or reported deaths or serious injuries, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

36626–36650 of 40449

HighFDA (Devices)·Z-0798-2014·2014-01-29
Carestream DRX-Evolution and Kodak DirectView DR 7500 X-Ray Systems Recalled
Carestream Health is recalling DRX-Evolution and Kodak DirectView DR 7500 diagnostic x-ray systems due to a potential for unexpected device movement.
Product
DR 7500 with FF WS These products are permanently installed diagnostic x-ray systems composed of 4 main components: an operator console, over head tube crane, x-ray tube assembly including a collimator and stationary generator. In addition the device can use an x-ray table…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0805-2014·2014-01-29
Sorin Orchestra Programmer Overestimates Pacemaker Battery Life
Sorin Group Italia is notifying physicians that its Orchestra programmer may overestimate the residual longevity of specific implanted pacemakers.
Product
ORCHESTRA/ORCHESTRA PLUS Programmer
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0785-2014·2014-01-29
Philips Recalls ADAC Gamma Camera Systems Due to Fork Joint Crack Risk
Philips Medical Systems is recalling ADAC ARGUS and CIRRUS Gamma Camera Systems because routine maintenance may fail to detect small cracks in the fork weldments.
Product
ADAC ARGUS Gamma Camera Systems & ADAC CIRRUS Gamma Camera Systems. Distributed by Philips Medical Systems, Cleveland, OH
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0808-2014·2014-01-29
GE Healthcare Recalls TRAM Modules Due to Intermittent ECG Noise
GE Healthcare is recalling 1,948 TRAM Modules because movement of the ECG cable connector causes intermittent noise on ECG and respiration waveforms, potentially reducing monitoring performance.
Product
GE Healthcare, TRAM MODULE, High-acuity patient monitoring. Product Usage: The TRAM Module is intended to provide uninterrupted monitoring of physiologic parameter data on adult, pediatric and neonatal patients during transport from one area of the hospital or facility, and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0782-2014·2014-01-29
Ranir Recalls UP & UP Kids' Power Toothbrushes Due to Choking Hazard
Ranir is recalling UP & UP and TopCare kids' power toothbrushes because the tufted disk may detach, posing a choking hazard to children three and younger.
Product
UP & UP kids' power toothbrush
Category
Consumer Product
Distribution
2 states
HighFDA (Devices)·Z-0810-2014·2014-01-29
Medrad Recalls Veris MR Monitor Units Due to Faulty Main Board
Medrad is recalling 922 Veris MR Monitor units because a faulty main board may cause unexpected system shutdowns, resulting in the loss of vital signs information.
Product
Medrad Veris MR Monitor units The system is intended to monitor physiological parameters of patients within any healthcare environment. The user, responsible to interpret the monitored data made available, will be a professional healthcare provider. Physiological data, gas…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0823-2014·2014-01-29
Siemens CentraLink Software Recall for Potential Patient Data Release Error
Siemens is recalling CentraLink Data Management System software versions 14.0.4, 14.0.5, and 14.0.8 because a disabled patient result may be released without proper review.
Product
Siemens CentraLink" Data Management System V14.0.4, V14.0.5 or V14.0.8 The CentraLink system software is a network solution provider and multi-system data manager for the instruments and lab automation systems (LAS) within the lab. The CentraLink software consolidates data…
Category
Medical Device
Distribution
3 states
HighFDA (Devices)·Z-0786-2014·2014-01-29
Siemens Recalls SimView NT Radiation Therapy Simulation Systems
Siemens is recalling 65 SimView NT radiation therapy simulation systems worldwide because a rare mechanical failure could prevent the stopping of intended component movements.
Product
SIMVIEW NT and SIMVIEW NT with IDI: October 01, 2012 Siemens ceased Simview distribution. Manufactured by: Mecaserto now known as Mecasim Parc de lEsplanade 9,Rue Niels Bohr 77400 Saint Thibault des Vignes- France The intended use of the SIEMENS branded SIMVIEW NT…
Category
Medical Device
Distribution
7 states
HighFDA (Devices)·Z-0804-2014·2014-01-29
GE Healthcare Recalls X-Ray Systems with Missing Monitor Suspension Screws
GE Healthcare is recalling 5,651 X-ray systems worldwide because four outer screws holding the overhead video monitor suspension may be missing. No monitor falls have been reported.
Product
Video Monitor Suspensions that may be on the following Fluoroscopic and Radiographic X-Ray systems: Precision 500D, Legacy, Prestilix, Monitrol, RFX, SFX, Tilt-C, Prestige VH, Prestige SI, and Prestige SII Product Usage: The systems are intended to be used as a universal…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0818-2014·2014-01-29
Siemens Recalls Dimension Vista Cyclosporine Flex Reagent Cartridges
Siemens Healthcare Diagnostics is recalling 1,586 Dimension Vista Cyclosporine Flex reagent cartridges due to complaints about variability in quality control and patient results.
Product
Dimension Vista Cyclosporine Flex reagent cartridge an in vitro diagnostic test for the quantitative measurement of cyclosporine A (CSA) in human whole blood on the Dimension Vista System. Measurements are used as an aid in the management of heart, liver, and kidney…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0796-2014·2014-01-29
Carestream DRX-Evolution X-Ray Systems Recalled for Unexpected Movement
Carestream Health is recalling DRX-Evolution and Kodak DirectView DR 7500 systems due to a risk of unexpected device movement.
Product
DRX-Evolution with FF WS These products are permanently installed diagnostic x-ray systems composed of 4 main components: an operator console, over head tube crane, x-ray tube assembly including a collimator and stationary generator. In addition the device can use an x-ray…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0781-2014·2014-01-29
Ranir Recalls TopCare and Up & Up Kids Power Toothbrushes
Ranir is recalling TopCare and Up & Up kids' power toothbrushes because the tufted disk may detach, posing a choking hazard to children three and younger.
Product
TopCare Clifford THE BIG RED DOG power toothbrush for kids!
Category
Consumer Product
Distribution
2 states
HighFDA (Devices)·Z-0806-2014·2014-01-29
GE Healthcare Recalls Dash Patient Monitors Due to ECG Noise
GE Healthcare is recalling Dash 3000, 4000, and 5000 patient monitors because cable movement causes intermittent noise on ECG and respiration waveforms, potentially reducing detection performance.
Product
GE Healthcare, Dash 3000, Dash 4000 and Dash 5000. Product Usage: The intended use of the system is to monitor physiologic parameter data on adult, pediatric and neonatal patients. K073462: The Dash 3000/4000/5000 patient monitor is intended for use under the direct…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0793-2014·2014-01-29
Remel Recalls Oxoid Norfloxacin Antimicrobial Susceptibility Test Discs
Remel Inc is recalling Oxoid Norfloxacin 10 mcg antimicrobial susceptibility test discs because some cartridges may contain discs not impregnated with the antibiotic.
Product
Oxoid Antimicrobial Susceptibility Test Discs, Norfloxacin 10 mcg., CT0434B, packaged in cartridges of 50 discs, 5 cartridges/pack. The firm name on the label is Oxoid Ltd., Basingstoke, Hampshire, England. Used in the semi-quantitative agar diffusion test method for in-vitro…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0783-2014·2014-01-29
Zimmer Segmental Systems Polyethylene Inserts Recalled for Loading Instructions
Zimmer, Inc. is recalling Segmental Systems Polyethylene Inserts to update surgical instructions regarding excessive loading risks.
Product
Zimmer Segmental Systems; Polyethylene Inserts, Size B. Designed to address significant bone loss resulting from oncology, trauma, and/or salvage of previously failed arthroplasty.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0822-2014·2014-01-29
Puritan Bennett Ventilator Manual Labeling Correction for Oxygen Sensor Life
Nellcor Puritan Bennett is correcting operator and service manuals for PB700 and PB840 ventilators to clarify the operational life of the oxygen sensor.
Product
Puritan Bennett 700 Series Ventilators (PB740 and PB760) PB700 Series Operators Manual: PN 10066984 & PN G-061874-00 and PB700 Series Service Manual: PN 10070389 The intended use of the oxygen sensor is to provide the oxygen concentration of the delivered gas at the patient…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0792-2014·2014-01-29
Remel Recalls Oxoid Cefpodoxime Antimicrobial Susceptibility Test Discs
Remel Inc is recalling Oxoid Cefpodoxime 10 mcg. Antimicrobial Susceptibility Test Discs because some cartridges may contain discs not impregnated with antibiotic.
Product
Oxoid Antimicrobial Susceptibility Test Discs, Cefpodoxime 10 mcg., CT1612B, packaged in cartridges of 50 discs, 5 cartridges/pack. The firm name on the label is Oxoid Ltd., Basingstoke, Hampshire, England. Used in the semi-quantitative agar diffusion test method for in-vitro…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0820-2014·2014-01-29
FDA Recalls Composix L/P Mesh Due to Labeling Mismatch
Davol, Inc. is recalling 46 units of Composix L/P Mesh with Echo PS Positioning System because the product labeling does not match the product configuration.
Product
Composix L/P with Echo PS 6" X 8" Product Code 0144680 The Composix L/P Mesh with Echo PS Positioning System is a non-absorbable sterile lightweight mesh prosthesis, with a preattached removable positioning system. This system is indicated and designed for the reconstruction…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0795-2014·2014-01-29
Remel Recalls Oxoid Ertapenem Antimicrobial Susceptibility Test Discs
Remel Inc is recalling Oxoid Ertapenem 10 mcg. Antimicrobial Susceptibility Test Discs because some cartridges may contain discs not impregnated with antibiotic.
Product
Oxoid Antimicrobial Susceptibility Test Discs, Ertapenem 10 mcg., CT1761B, packaged in cartridges of 50 discs, 5 cartridges/pack. The firm name on the label is Oxoid Ltd., Basingstoke, Hampshire, England. Used in the semi-quantitative agar diffusion test method for in-vitro…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0817-2014·2014-01-29
Ortho-Clinical Diagnostics Recalls VITROS Chemistry Products COCM Reagent
Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products COCM Reagent because of inaccurate quality control results. The recall affects 3,342 units distributed worldwide.
Product
VITROS Chemistry Products COCM Reagent
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0815-2014·2014-01-29
Bard Access Systems Recalls Low Profile Ports with Undersized Catheters
Bard Access Systems is recalling Low Profile Ports with 6.6 Fr catheters because some silicone catheters may be undersized to 5.3 Fr.
Product
Titanium Single Lumen Low-Profile port, with Pre-Attached open-Ended Silicone 6.6Fr Catheter. Product Code 0602180 Usage: The 6.6 Fr Open-Ended Single-Lumen venous catheters is packaged into various Bard Acess Systems finished goods as Attachable or Preconnected catheters in…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0814-2014·2014-01-29
Bard Access Systems Recalls MRI Low Profile Ports with Undersized Catheters
Bard Access Systems is recalling MRI Low Profile Single Lumen ports because some silicone catheters may be undersized to 5.3 Fr instead of the labeled 6.6 Fr.
Product
MRI Low Profile Single Lumen port with Open-Ended 6.6Fr Silicone Catheter. Product Code 0603880. Product Usage: The 6.6 Fr Open-Ended Single-Lumen venous catheters is packaged into various Bard Acess Systems finished goods as Attachable or Preconnected catheters in BardPort…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0799-2014·2014-01-29
Zeiss Compensator Slider Lambda 6x20 Recalled for Misalignment
Carl Zeiss Microscopy is recalling the Compensator Slider Lambda 6x20 component due to misalignment of the lambda plate.
Product
Compensator Slider Lambda 6x20 component (part number 473704-0000-000) utilized on all upright ZEISS microscopes (Axio Imager, Axio Scope. A1, Axio Lab. A1). Component used to determine composition of urinary calculi, urinary sediments, bio-crystallates and diagnosis of…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0803-2014·2014-01-29
Civco Belly Board MRI Recalled Due to Misaligned Scales
Civco Medical Instruments is recalling specific lots of Belly Board MRI devices because scales may be misaligned, potentially affecting measurement accuracy.
Product
Civco Belly Board MRI, Reusable non-sterile glass fiber belly board with cushion, REF 126000, packaged 1 per box. Product Usage: This device is intended to reduce the irradiated small bowel volume of gynecological patients undergoing treatment in the pelvic region.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0802-2014·2014-01-29
Civco Belly Board Recalled Due to Misaligned Scales
Civco Medical Instruments is recalling 138 belly boards because scales may be misaligned from the zero reference, potentially affecting measurement accuracy.
Product
Civco Belly Board, Reusable non-sterile carbon fiber belly board with cushion, REF 125012, packaged 1 per box. Product Usage: This device is intended to reduce the irradiated small bowel volume of gynecological patients undergoing treatment in the pelvic region.
Category
Medical Device
Distribution
Distributed nationwide

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36626–36650 of 40449