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Forceps irrigation plug

Official notice

27 Dec 2024

Last checked

27 Dec 2024

Critical riskHealth Canada

An official Health Canada notice concerns Forceps irrigation plug. Olympus' investigation into reported infection and contamination complaints associated with the MAJ-891 revealed a potential risk of patient infection due to inadvertent retention of biomaterial when the reprocessing procedure for the MAJ-891 is not performed as instructed, such as not disconnecting the MAJ-891 from the endoscope and disassembling it before reprocessing. In the period of August 1, 2021 to May 1, 2024, Olympus identified one-hundred and twenty (120) serious injuries and one (1) death reported due to infection following procedures in which the MAJ-891 was used with a cystoscope (CYF scope). Investigation by Olympus indicates that there was improper reprocessing in most of these infection cases. Olympus has not received any infection-related complaints for cases where the MAJ-891 was used with other compatible endoscopes including ureteroscopes (URF series), choledochoscopes (CHF series), hysteroscopes (HYF series), and ventriculoscopes (VEF series), although it should be noted that the risk of infection as a result of improper reprocessing is also applicable to these endoscopes. Due to the risk of infection that may result from improper MAJ-891 reprocessing, alternatives to the MAJ-891 should be used instead. A list of Olympus alternative irrigation plugs that can be used with certain Olympus scopes is listed in the supplied medical device recall letter. If no alternative for the MAJ-891 is available, Olympus is reminding customers to closely follow the reprocessing instructions as indicated in the instructions for use. Olympus is also reminding users to inspect the biopsy valve (MAJ-579), used as illustrated in the letter in the MAJ-891 for damage or deformation and replace the biopsy valve if damage is identified. A damaged or deformed biopsy valve may impact the efficacy of reprocessing. Recall start date: December 20, 2024 Published 2024-12-27.

What to do now

Contact the manufacturer if you require additional information.

Recall number

76768

Official notice

2024-12-27

The hazard

Olympus' investigation into reported infection and contamination complaints associated with the MAJ-891 revealed a potential risk of patient infection due to inadvertent retention of biomaterial when the reprocessing procedure for the MAJ-891 is not performed as instructed, such as not disconnecting the MAJ-891 from the endoscope and disassembling it before reprocessing. In the period of August 1, 2021 to May 1, 2024, Olympus identified one-hundred and twenty (120) serious injuries and one (1) death reported due to infection following procedures in which the MAJ-891 was used with a cystoscope (CYF scope). Investigation by Olympus indicates that there was improper reprocessing in most of these infection cases. Olympus has not received any infection-related complaints for cases where the MAJ-891 was used with other compatible endoscopes including ureteroscopes (URF series), choledochoscopes (CHF series), hysteroscopes (HYF series), and ventriculoscopes (VEF series), although it should be noted that the risk of infection as a result of improper reprocessing is also applicable to these endoscopes. Due to the risk of infection that may result from improper MAJ-891 reprocessing, alternatives to the MAJ-891 should be used instead. A list of Olympus alternative irrigation plugs that can be used with certain Olympus scopes is listed in the supplied medical device recall letter. If no alternative for the MAJ-891 is available, Olympus is reminding customers to closely follow the reprocessing instructions as indicated in the instructions for use. Olympus is also reminding users to inspect the biopsy valve (MAJ-579), used as illustrated in the letter in the MAJ-891 for damage or deformation and replace the biopsy valve if damage is identified. A damaged or deformed biopsy valve may impact the efficacy of reprocessing. Recall start date: December 20, 2024

How to check if you're affected

Compare the product name and identifiers below with the item you own. Follow the official notice if they match.

Recall Numbers

76768

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Affected products

Product 1

Affected products - Forceps/Irrigation Plug, Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - MAJ-891

Risk / hazard

Olympus' investigation into reported infection and contamination complaints associated with the MAJ-891 revealed a potential risk of patient infection due to inadvertent retention of biomaterial when the reprocessing procedure for the MAJ-891 is not performed as instructed, such as not disconnecting the MAJ-891 from the endoscope and disassembling it before reprocessing. In the period of August 1, 2021 to May 1, 2024, Olympus identified one-hundred and twenty (120) serious injuries and one (1) death reported due to infection following procedures in which the MAJ-891 was used with a cystoscope (CYF scope). Investigation by Olympus indicates that there was improper reprocessing in most of these infection cases. Olympus has not received any infection-related complaints for cases where the MAJ-891 was used with other compatible endoscopes including ureteroscopes (URF series), choledochoscopes (CHF series), hysteroscopes (HYF series), and ventriculoscopes (VEF series), although it should be noted that the risk of infection as a result of improper reprocessing is also applicable to these endoscopes. Due to the risk of infection that may result from improper MAJ-891 reprocessing, alternatives to the MAJ-891 should be used instead. A list of Olympus alternative irrigation plugs that can be used with certain Olympus scopes is listed in the supplied medical device recall letter. If no alternative for the MAJ-891 is available, Olympus is reminding customers to closely follow the reprocessing instructions as indicated in the instructions for use. Olympus is also reminding users to inspect the biopsy valve (MAJ-579), used as illustrated in the letter in the MAJ-891 for damage or deformation and replace the biopsy valve if damage is identified. A damaged or deformed biopsy valve may impact the efficacy of reprocessing. Recall start date: December 20, 2024

Where it was sold

The source does not list specific retailers. See the official notice for where affected products were sold.

Location 1

CA · Canada

Affected area 1

CA · Canada

Company & contacts

Manufacturer

Not provided

Phone

Not provided

Brand: Olympus Medical, Forceps Irrigation Plug.

Source & status

Source

Health Canada

Tier

official

Category

HOME

Classification

Type I

App estimate

critical

Recall details

Recall number

76768

Classification

Type I

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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