The Recall Desk

Manufacturer

Baylis Medical Company Inc.

3 recalls in our database name Baylis Medical Company Inc. as the manufacturing or recalling firm.

What the numbers show

Total
3
Critical
0
Severe
0
Most recent
2020-05-27

Of the 3 recalls from Baylis Medical Company Inc. we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) are Severe.

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

1–3 of 3

  • HighFDA (Devices)·Z-2070-2020·2020-05-27

    Baylis Medical Recalls NRG RF Transseptal Kits Due to Packaging Defect

    Baylis Medical is recalling NRG RF Transseptal Kits because sterile packaging may be compromised during shipping, posing a remote risk of infection.

    Product
    NRG RF Transseptal Kit; Model No.s : NTK-710-8545, NTK-710-8555, NTK-711-8545, NTK-711-8555, NTK-711-8590, NTK-P711-8545, NTK-P711-8555, NTK-710-8545S, NTK-710-8555S, NTK-711-8545S, NTK-711-8555S, NTK-710-8545N, NTK-711-8545N and NTK-711-8555N.
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2069-2020·2020-05-27

    Baylis Medical Recalls TorFlex Transseptal Guiding Sheaths Due to Packaging Defects

    Baylis Medical is recalling TorFlex Transseptal Guiding Sheaths because sterile packaging may be compromised during shipping, posing a remote risk of infection.

    Product
    TorFlex Transseptal Guiding Sheath ; Model numbers: TF8-32-63-45, TF8-32-63-55, TF8-32-63-90, TF8-32-63-135, TF85-32-63-37, TF85-32-63-45, TF85-32-63-55, TF85-32-63-90, TF85-32-63-135, TF8-32-81-45, TF8-32-81-55, TF8-32-81-90, TF85-32-81-37, TF85-32-81-45, TF85-32-81-55, and TF8
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0879-2013·2013-03-06

    Baylis Medical Recalls Unsealed Sterile RF Cannulas for Pain Relief

    Baylis Medical is recalling 1,780 sterile RF cannulas distributed to Australia because some pouches were not sealed, risking sterility loss.

    Product
    BMC RF Cannula Curved Sharp RadiOpaque, Non-Pyrogenic, Active Tip: 10mm, Gauge 16 Ga, Length: 100mm. The BMC RF Cannula is sealed in a Tyvek pouch (primary packaging) and then placed into a white shelf-box (secondary packaging) with the instructions for use. A predetermined num
    Category
    Medical Device
    Distribution
    0 states

About this company

Community-sourced company facts from Wikidata, not from any recall agency. This is background on the corporate entity — it says nothing about the recall(s) listed on this page, which come from the agency source notice above.

Baylis Medical (Canada)

company in Montreal, Canada

Country
Canada
Founded
1986

Official website

Source: Wikidata (Q30253567), licensed CC0. Wikidata is community-edited and may not reflect the current corporate structure.