The Recall Desk

Manufacturer

Summit Medical, Inc.

3 recalls in our database name Summit Medical, Inc. as the manufacturing or recalling firm.

What the numbers show

Total
3
Critical
0
Severe
0
Most recent
2015-12-23

Of the 3 recalls from Summit Medical, 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-0435-2016·2015-12-23

    Summit Medical Recalls AbsorbENT Nasal Packs Due to Missing Split

    Summit Medical is recalling specific lots of AbsorbENT nasal packs because the product lacks a required split in the packing.

    Product
    AbsorbENT, Sterile Compressed Absorbent Sponge, Nasal Pack, 8.9cm(L) x 3.0cm (W) x 1.5cm (H), RH-7413-10, Sterilized by Gamma Radiation, Rx only. Used as a nasal packing following intranasal surgery to absorb blood and other fluids in the nasal cavity.
    Category
    Medical Device
    Distribution
    1 state
  • LowFDA (Devices)·Z-1731-2014·2014-06-18

    Summit Medical Recalls Mixed Lot of Armstrong Grommet Ventilation Tubes

    Summit Medical, Inc. is recalling one lot of Armstrong Grommet ventilation tubes due to mixed flange types. The agency states this poses no health hazard to users or patients.

    Product
    Armstrong Grommet with wire Otological Ventilation Tube Catalog #: VT-0507-01, Sterilized by Ethylene Oxide, Rx Only. Intended to provide ventilation to the middle ear space through the tympanic membrane.
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1319-2013·2013-05-22

    Summit Medical Recalls Myringotomy Lance Blades Due to Incorrect Packaging

    Summit Medical is recalling Myringotomy Lance Blades because the boxes contain the wrong type of blade.

    Product
    Summit Medical, BL-2006, Myringotomy Lance (Juvenile) Blade, Sterile P, Summit Medical, Inc., 815 Northwest Parkway, Suite 100, St. Paul, MN 55121 Use to make an incision in the tympanic membrane.
    Category
    Medical Device
    Distribution
    4 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.

Summit Medical Group

company in Berkeley Heights, United States

Country
United States

Official website

Source: Wikidata (Q7637836), licensed CC0. Wikidata is community-edited and may not reflect the current corporate structure.