Steris Corporation recalls AMSCO 7052HP Washer/Disinfector Model/Catalog Number: 7052HP Product Description: The AMSCO 7052HP Washer/Disinfector is intended for use…
Wire connected to the electrical box may shift out of its intended position, which may result in electrical arcing. Electrical arcing remains internal within the unit (no risk of shock to users).
Read the official notice →- Date
- 2025-12-17
- Country
- United States
- Brand
- Steris
- Product
- AMSCO 7052HP Washer/Disinfector Model/Catalog Number: 7052HP Product Description: The AMSCO 7052HP Washer/Disinfector is intended for use…
- Classification
- Class II
- Units
- Worldwide - US Nationwide distribution in the states of Arizona, Colorado,…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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
- 2026-06-24
USSteris Corporation recalls HarmonyAIR A-Series Surgical Lighting System
The the plus and minus buttons (+/-) used to control light intensity on the light heads may detach.
- US
Steris Corporation recalls HarmonyAIR A-Series Surgical Lighting System
There is a potential for paint delamination (chipping/peeling) on the lighting system's light heads.
FDA · DeviceSteris CorporationWorldwide distribution - US Nationwide and the countries of Australia, Canada,…Official notice → - 2026-02-18
- US
Steris Corporation recalls Barco MNA with the HexaVue IP Integration System, Model/Catalog Number: MNA-6x0-H
This is a sub-recall of event RES 96885. The supplier identified that during their manufacturing process for a limited batch of MNA-6x0 (adapter) components the incorrect configuration file was used.
FDA · DeviceSteris CorporationUS Nationwide distribution in the states of FL, NC, NY, OH, TN, TX, and VA.Official notice → - 2025-08-06
- US
Steris Corporation recalls Dual Flat Panel Monitor (DFPM) accessories for HarmonyAIR E-Series Surgical Lighting Systems
The DFPM yoke assembly ("yoke assembly") may detach from the spring arm. Should the yoke assembly detach from the spring arm, the yoke assembly would not be expected to fully detach but rather hang from the wiring…
FDA · DeviceSteris CorporationWorldwide - US Nationwide and Puerto Rico and the country of Canada.Official notice → - 2024-08-14
- US
Steris 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 →
Other drugs & medical recalls in the United States
- 2025-12-17
- US
Datascope Corp. recalls Cardiosave Rescue. Intra-Aortic Balloon Pump system.
The IFU addendum revises the Preventative Maintenance schedule to align with the update introduced in the Service Manual as of June 2023.
FDA · DeviceDatascope Corp.Domestic: Nationwide Distribution; Foreign: Albania, Algeria, Angola,…Official notice → - US
Nipro Medical Corporation recalls Hemodialysis System, Surdial DX REF: MC+SDX01 Rx Only
Screw may loosen or fallout of Hemodialysis system
FDA · DeviceNipro Medical CorporationUS Nationwide distribution in the states of AL, AR, CA, FL, GA, IL, IA, MI,…Official notice → - US
Medline Industries, LP recalls DEXLOCK Achilles Repair Implant Kits, MAKT4520
There have been multiple complaints of drill bit fusing to the bushing/sleeve within the drill guide during use. Retrieving a replacement drill bit and drill guide may prolong the surgical procedure.
FDA · DeviceMedline Industries, LPUS Nationwide distribution in the states of AL, AR, AZ, CO, DE, FL, GA, ID,…Official notice → - US
C.R. Bard Inc recalls BD InLay Optima Ureteral Stent Kit Size: 6 Fr. x 30 cm, Ureteral Stent Kit REF 788630
Labeling discrepancy; Ureteral stent actual size may not match the actual product label.
FDA · DeviceC.R. Bard IncWorldwide - US Nationwide distribution in the states of AZ, CA, CO, FL, GA,…Official notice → - US
Medline Industries, LP recalls Quick Strip Fabric Sterile Adhesive Bandages, 1" x 3", Medline Item Number NON25660QS
Medline has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may exhibit open seals in the packaging which may compromise the sterility of the product.
- US
Cardinal Health 200, LLC recalls ChemoPlus gowns: Product Code Product Description CT5500T ChemoPlus Full Coverage Sleeve, Universal, Medium Blue, Non-sterile; CT5502T…
Affected gowns have the incorrect expiration date on the product packaging. Product has a shelf-life of three years which is mislabeled on the product packaging as five (5) years.
FDA · DeviceCardinal Health 200, LLCWorldwide distribution - US Nationwide and the country of Canada.Official notice →