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All product recalls associated with Steris Corp.
Total Recalls
1000
Past Year
353
Class I (Serious)
22
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.
The cables inside the pump conduit box may be exposed (not covered with wire nut and/or electrical tape) that could cause a potential electrical shock hazard.
This recall involves Laars 9600 CB Condensing Heating Boilers and Laars 9600 HWG Condensing Water Heaters with black vent pipe/tubing. The recalled boilers are used to generate hot water for heating systems including baseboards or radiant flooring. The recalled water heaters generate hot water for use in homes, such as showers, sinks and dishwashers. "Mark II" and "9600 CB" or "9600 HWG" are printed on the front of the boilers and water heaters. The model number and BTU size are printed on the right side of the unit. The recalled boiler and water heater exteriors are putty and black-colored or taupe and black-colored. Only the following models are included in this recall. Model Input (Btu/h) Gas Boilers: CB 150 150,000 CB 175 175,000 CB 200 200,000 Water Heaters: HWG 150 150,000 HWG 175 175,000 HWG 200 200,000
The Collimator field-defining light beam does not meet the light field contrast ratio requirement of 4:1. System is non-compliant with performance standard (1020.31 (d)(2)(iii) 21 CFR
Localization error; with planning data transferred to the Optical Guidance Platform via DICOM RT; The software incorrectly computes the center of the CT volume, resulting in a potential axial error ranging from 0.3 mm to 1.5 mm, affecting both Fractionated and Stereotactic Radiosurgery (SRS) Treatments
Premature wear; The material from which the hex driver was made was improperly hardened during manufacturing and could lead to premature wear.
Premature Wear; The material from which the hex driver was made was improperly hardened during manufacturing and could lead to premature wear.
Premature Wear; The material from which the hex driver was made was improperly hardened during manufacturing and could lead to premature wear.
A software anomaly in a medical device used for patient treatment could result in accidental or unintended exposure radiation exposure. The tilt rotation compensation algorithm does not adequately compensate for the tilt rotation.
The current package insert for the AmpliChip CYP 450 test, lists an incorrect part number for DNase I. The DNase is listed in the "Other Materials Required" section as 'DNase I rec., RNase-free, P/N 04716728001 (Roche Applied Science)" . The Part Number listed for the DNase I listed is incorrect and of lower specific activity than the correct/validated DNase.
The current package insert for the AmpliChip CYP 450 test, lists an incorrect part number for DNase I. The DNase is listed in the "Other Materials Required" section as 'DNase I rec., RNase-free, P/N 04716728001 (Roche Applied Science)" . The Part Number listed for the DNase I listed is incorrect and of lower specific activity than the correct/validated DNase.
This recall involves the Weber® Genesis® 320™ Series gas grills which are designed to be used with either natural gas or with liquid propane gas tanks, and are equipped with a flush-mounted side burner accessory. The gas hose is made of stainless steel. The grills are sold in stainless steel and in black, blue or green porcelain enamel. All serial numbers begin with the prefix "DI". The model and serial number are located on the tank blocker/drip pan holder located inside the storage cart. Only the following product names and model numbers are included in this recall: Product Name Model Numbers Genesis® E-320™ 3751001; 3757001; 3758001; 3851001 Genesis® S-320™ 3780001; 3880001 Genesis® EP-320™ 3751301; 3752301; 3757301; 3758301; 3851301 Genesis® ESP-320™ 3750101; 3750201; 3850101 Genesis® CEP-320™ (Sold in Canada Only) 3751701; 3752701; 3851701
LIFEPAK CR Plus defibrillators with software version 1.16 or lower may miscalculate the HLC battery capacity and result in the CHARGE-PAK battery charger icon/indicator to display and falsely indicate battery needs replacement.
During routine service, primary and/or secondary collimators may not have been properly reinstalled.
During routine service, primary and/or secondary collimators may not have been properly reinstalled.
Incorrect simulation and/or beam placement: An anomaly has been identified with the Philips VoxelQ workstation utlizing AcQPlan software version 4.2, 4.2.1, 4.9, 4.9.1, 4.9.2, 4.9.3, 5.0, 5.0.1, 5.0.2 or 5.0.3 when computing absolute patient marking coordinates with data containing reconstruction offsets from the Mx800, the Mx8001DT, and the Brilliance 6, 10, 16, 16P, and Big Bore CT systems. Whe
During routine service, primary and/or secondary collimators may not have been properly reinstalled.
During routine service, primary and/or secondary collimators may not have been properly reinstalled.
During routine service, primary and/or secondary collimators may not have been properly reinstalled.
During routine service, primary and/or secondary collimators may not have been properly reinstalled.
During routine service, primary and/or secondary collimators may not have been properly reinstalled.