Public recall detail

RAPICIDE™ PA High Level Disinfectant

2026-09-17

medium
Health products Health product recall
Quick summary

Quick summary: RAPICIDE™ PA High Level Disinfectant. Reason: Health product recall. Category: Health products. Date: 2026-09-17.

Recommended action

Recommended action: compare your product with the official notice and follow the instructions published by the official source.

Recall details

Quick summary: RAPICIDE™ PA High Level Disinfectant. Reason: Health product recall. Category: Health products. Date: 2026-09-17.

Official details

Affected product details

Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.

BrandMedivators Inc.
ProductRAPICIDE™ PA High Level Disinfectant
IssueMedical devices - Performance
Recall classType II
IdentificationRA-82643

Affected products

ProductRAPICIDE™ PA High Level Disinfectant
Lot689982
ModelML02-0116
Serial number689982
DescriptionRAPICIDE™ PA High Level Disinfectant
ProductRAPICIDE™ PA High Level Disinfectant
Lot690994
ModelML02-0116
Serial number690994
DescriptionRAPICIDE™ PA High Level Disinfectant
ProductRAPICIDE™ PA High Level Disinfectant
Lot689172
ModelML02-0116
Serial number689172
DescriptionRAPICIDE™ PA High Level Disinfectant
ProductRAPICIDE™ PA High Level Disinfectant
Lot692571
ModelML02-0116
Serial number692571
DescriptionRAPICIDE™ PA High Level Disinfectant
ProductRAPICIDE™ PA High Level Disinfectant
Lot691740
ModelML02-0116
Serial number691740
DescriptionRAPICIDE™ PA High Level Disinfectant
ProductRAPICIDE™ PA High Level Disinfectant
Lot694358
ModelML02-0116
Serial number694358
DescriptionRAPICIDE™ PA High Level Disinfectant

Issue

STERIS identified through customer complaints that a small number of RAPICIDE™ Part A bottles within certain lots may begin to bulge or expand over time. Part A is the active component of chemistry that creates peracetic acid, which may off-gas during the shelf-life of the product. Under routine conditions, the Part A bottle cap includes a vent intended to allow gas to escape (off-gassing) and reduce the potential for gas accumulation. If the vented cap becomes blocked, gas may accumulate and the bottle may swell due to increased internal pressure. In some cases, excess vapor or liquid chemistry may escape from the bottle when the cap is twisted during opening, which could result in user exposure if required personal protective equipment (PPE) is not properly used. Such exposure may result in injury to the user or others in close proximity.STERIS will provide a customer notification letter to all consignees who purchased affected lots. Consignees will be requested to follow the appropriate procedures and PPE needed to address any swollen bottles. The chemistry itself remains safe and effective to use in accordance with its labeling. However, replacement product will be provided for any product that had to be disposed.

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - General hospital and personal use
CompaniesMedivators Inc. 14605 28th Avenue North, Minneapolis, Minnesota, United States, 55447
Recall date2026-09-08
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-82643
Background{}
CompaniesMedivators Inc. 14605 28th Avenue North, Minneapolis, Minnesota, United States, 55447
AudiencesHealthcare
Source updated2026-09-17

Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.

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