Every recall we track for Gentell, Inc — 11 in all — plus the complaints and injury reports the public filed about them.
Gentell recalls 100% honey wound dressings due to improper FDA registration. Affected lots include 1133718, 1135318, and others. Consumers should check product labels for lot numbers.
Gentell Honey Hydrogel 4oz tubes (model GEN-11340) were recalled due to improper FDA registration. This affects specific lot numbers for wound dressings used on minor wounds and ulcers.
Gentell recalls honey hydrogel wound dressings due to improper FDA registration. Affected lots include 1133718, 1135318, and others. No action needed as the product is safe but must be registered with FDA.
Gentell recalls 100% honey wound dressings due to improper FDA registration. Affected products include specific model numbers and lot ranges. Consumers should contact the company for details.
Gentell Hydrogel Ag 4x8 (model GEN-11820) is recalled due to improper FDA registration. This product is used for wound care under healthcare supervision. No action is required as the issue is a registration error, not a safety hazard.
Gentell recalls Hydrogel Ag 2x2 model GEN-11220 due to improper FDA registration. Product used under healthcare professional supervision for wound care. No immediate action needed as it's a registration issue, not a safety hazard.
Gentell recalls 4oz Hydrogel Ag tubes due to improper FDA registration. This affects wound care products used under healthcare professional supervision.
Gentell Hydrogel Ag 4x4 (model GEN-11420) is recalled due to improper FDA registration. This product is used for wound care under healthcare supervision. Consumers should contact the manufacturer for details.
