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H&H Big Cinch Abdominal Bandage

H&H MEDICAL CORPORATION · Model 1 · UDI-DI 00857048006064

FQM
10
510(k) clearances
297
Adverse events
30
Recalls
698
Facilities

Description

With a 12 in. x 16 in. ABD Pad capable of covering the largest wound areas, the Big Cinch protects vital abdominal organs and large wounds to keep them protected and provide hemorrhage control. The Big Cinch easily secures to the abdomen, leg, or other large area with over 5 feet of 4 in wide strengthened elastic wrap sewn onto the large ABD Pad. The pad and the wrap ensure a tight fit to to prevent slipping while gently protecting the delicate abdominal region. The Big Cinch comes in a sterile, vacuum-sealed 5 mil barrier bag, flat folded to create a small tight package.

Recalls

DateFirmReason
2026-02-27Medline Industries, LPFirm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
2025-03-03MEDLINE INDUSTRIES, LP - NorthfieldThere is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
2024-04-08MEDLINE INDUSTRIES, LP - NorthfieldMedical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that ma
2024-04-02Andover Healthcare Inc.A packaging seal gap could impact the sterility of the product.
2022-06-22ASO LLCThe product falls apart during handling after removal from its primary packaging.
2022-05-25Mckesson Medical-Surgical Inc. Corporate OfficeFacility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 0
2022-02-01BSN Medical IncThe folding boxes within the shipping case are mislabeled. The shipping case and immediate packages within the folding boxes are correctly labeled.
2020-08-21North American Rescue LLC.Lack of sterility assurance of the 30-0171
2019-06-19Andover Healthcare Inc.Incomplete packaging seal of sterile product
2019-06-19Andover Healthcare Inc.Incomplete packaging seal of sterile product

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.