Steris Corporation recalls Hookup Accessories used with MEDIVATORS ADVANTAGE PLUS and ADVANTAGE PLUS Pass Thru Automated Endoscope Reprocessors Model # Model…
Identification label on affected hookups could become illegible over time due to the label's ink coming off. This may potentially prevent users from being able to effectively identify the hookup and may ultimately…
Read the official notice →- Date
- 2024-01-03
- Country
- United States
- Brand
- Steris
- Product
- Hookup Accessories used with MEDIVATORS ADVANTAGE PLUS and ADVANTAGE PLUS Pass Thru Automated Endoscope Reprocessors Model # Model…
- Classification
- Class II
- Units
- Domestic distribution nationwide. Foreign distribution to Australia Canada…
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More Steris recalls
- 2024-08-14
USSteris Corporation recalls Hookup Model/Catalog Number: 2-8-540CAS Product Description: Hookups provide the interface between an Advantage Plus" Automated Endoscope…
IFU for hookup were incorrectly reflected within hookup IFUs and online reference system, Hookup Lookup (HULU). Use of an incorrect hookup connection and/or parameter set may prevent an endoscope from being properly…
FDA · DeviceSteris CorporationWorldwide distribution - United States Nationwide and the countries of Canada,…Official notice →- 2024-02-14
- US
Steris Corporation recalls Dual Articulating Headrest, Pad Ret P/N P141210805, REF BF754
Dual-articulating head rest may not stay in place or may fail to lock into position during a patient procedure which could result in an injury to the patient or a procedural delay.
FDA · DeviceSteris CorporationWorldwide - US Nationwide distribution in the states of AZ, CA, FL, IL, IN,…Official notice → - 2024-01-24
- US
Steris Corporation recalls V. Mueller Universal Bandage Scissors Black Plastic Handles Heavy-Duty, Autoclavable, Overall Length 7 (18 cm)- Intended to cut through…
Bandage Scissors handle cover component contains an incorrect color masterbatch resin carrier. This may allow a pink dye/residue to appear on the Bandage Scissors and/or sterilization pouches after processing.
- 2023-05-24
- US
Steris Corporation recalls Reliance Vision Multi-Chamber Washer/Disinfector, Reference Number FH83062
In the remote occurrence in which the electrical contactor component present in the drying chambers of the Reliance Vision Multi-Chamber Washer/Disinfector malfunctions, the heating elements in the drying chamber could…
FDA · DeviceSteris CorporationWorldwide Distribution: US (Nationwide) and OUS (Foreign) to countries of:…Official notice → - 2023-05-10
- US
Steris Corporation recalls Steris Lighting and Visualization Systems, Sterile Light Handle Cover (LB53)- Surgical light handle covers, including disposable surgical…
Light handle covers may separate from the light handle (detach and fall off) during use, this could result in a procedure delay and/or impact the sterile field which could result in an injury to the patient
FDA · DeviceSteris CorporationWorldwide - US Nationwide distribution including Puerto Rico and the countries…Official notice → - 2023-01-11
- US
Steris Corporation recalls VERIFY Steam Test Pack (20 Tests and 20 controls) Item Number: S3069 Intended for use in installation testing and routine monitoring of…
Biological indicator (BI) used to promote growth of the G. stearothermophilus and B. atrophaeus spores was inconsistent in promoting growth throughout lot , some BIs within the lot performed as intended while others…
FDA · DeviceSteris CorporationNationwide Foreign: AE AT CA CO ES FI GU IN IT JP MX SG TH TW ZAOfficial notice →
Other drugs & medical recalls in the United States
- 2024-01-03
- US
Atrium Medical Corporation recalls Atrium Oasis Drain Single W / AC, Part No. 3600-100
A sterilization nonconformance prematurely aged the product by 48.3 days, resulting in the expiration date on the label not being accurate. This nonconforming product was inadvertently distributed to customers.…
FDA · DeviceAtrium Medical CorporationDomestic distribution nationwide. No foreign distribution.Official notice → - US
Fresenius Medical Care Holdings, Inc. recalls Liberty Select Cycler, Model numbers RTLR180343 and RTLR180111
Affected Liberty Select cyclers may display an incorrect time stamp on the treatment data report sent to the clinic.
FDA · DeviceFresenius Medical Care Holdings, Inc.US Nationwide distribution in the states of AL, CA, FL, IL, IN, LA, MI, MO,…Official notice → - US
Acumed LLC recalls RibLoc U Plus 90 Instrument PRIMARY GUIDE ASSY, LOW PROFILE REF RBL2320 The RBL2320, Low Profile Primary Guide is an instrument used with…
Due to potential breakage during use.
FDA · DeviceAcumed LLCWorldwide - U.S. Nationwide distribution including in the states of AL, AZ,…Official notice → - US
Landauer recalls Landauer microSTARii reader, Medical Dosimetry System, Model Numbers: 18000-000/18001-000/18007-000
MicroSTARii readers may be contributing to the nanodot dosimeter measurement inaccuracy in two possible ways. The first is related to the interaction of the reader s LED beam profile with the nanoDot dosimeter. The…
FDA · DeviceLandauerUS and Australia, Brazil, Canada, China, France, Germany, India, Japan,…Official notice → - US
Medtronic Neuromodulation recalls Medtronic SynchroMed II, Model 8637-20, Programmable pump
Medtronic recently identified that if the SynchroMed II pump switches into telemetry mode due to electromagnetic interference (EMI) from an MRI scan, while the pump is sounding an alarm, the pump will not resume drug…
- US
Abbott Laboratories recalls Alinity ci-series System Control Module, REF: 03R70-01
There are potential performance issues found in the Alinity ci-series System software versions 3.4.0 and lower, including: 1) SCC Reagent load error during daily maintenance; 2) Sample Laboratory Report error; 3)…
FDA · DeviceAbbott LaboratoriesUS: AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA,…Official notice →