The Recall Desk

Manufacturer

Beevers Manufacturing & Supply, Inc.

3 recalls in our database name Beevers Manufacturing & Supply, Inc. as the manufacturing or recalling firm.

What the numbers show

Total
3
Critical
0
Severe
0
Most recent
2014-12-10

Of the 3 recalls from Beevers Manufacturing & Supply, 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

  • ModerateFDA (Devices)·Z-0487-2015·2014-12-10

    Beevers Cannulaide Model 101 Recalled for Incorrect Labeling

    Beevers Manufacturing recalled 393 units of Cannulaide Model 101 because the product was packed and labeled as Model 102.

    Product
    Cannulaide, Model 101. The Cannulaide product is composed of die-cut hydrocolloid coated polyurethane film with an integral hook strip (i.e., Velcro) to allow for the use of a loop material to help secure a nasal interface. The Cannulaide is applied under and over the nose o
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0483-2015·2014-12-03

    Beevers Cannulaide Respirator Recalled for Improper Pouch Seal

    Beevers Manufacturing recalled Cannulaide respirators due to improper pouch seals that could affect device shelf life.

    Product
    Cannulaide, Model 101, 102, 103. Respirator. The Cannulaide product is composed of die-cut hydrocolloid-coated polyurethane film with an integral hook strip (i.e., Velcro) to allow for the use of a loop material to help secure a nasal interface. The Cannulaide is applied
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-2181-2014·2014-08-20

    Beevers Recalls Luma Wrap Phototherapy Swaddlers for Regulatory Misclassification

    Beevers Manufacturing is recalling Luma Wrap neonatal phototherapy swaddlers because they were marketed without a required FDA 510(k) clearance.

    Product
    Luma Wrap Phototherapy Swaddler is designed to provide centered and comfortable boundaries as a benefit for restive babies in the Neonatal Intensive Care Unit.
    Category
    Medical Device
    Distribution
    0 states