Washington recalls

16F dual-valved splittable sheath introducer due to a design defect, may not split as intended, which may result in hemorrhage, foreign bodies, procedure delay, embolization/thrombosis, impaired catheter function, loss of vessel for future vascular access.

Probes may rupture/burst during activation

Probes may rupture/burst during activation

Probes may rupture/burst during activation

Undeclared Allergen - Wheat and Soy (from Soy Lecithin). The ingredient statement and allergen information do not include wheat or soy.

Metal fragments. The potential foreign object is a hard, metal (stainless steel), curled spring. Dimensions of a similar spring measure 2.27mm in cross-sectional thickness and 25.38mm in coil width. Spring ends are not sharp but may be sharp if broken/ cut.

Potential adulteration with erucic acid from mustard oil ingredient.

Potential adulteration with erucic acid from mustard oil ingredient.

Potential adulteration with erucic acid from mustard oil ingredient.

Potential adulteration with erucic acid from mustard oil ingredient.

Potential adulteration with erucic acid from mustard oil ingredient.

Potential adulteration with erucic acid from mustard oil ingredient.

Foreign material (aluminum pieces).

Foreign material (aluminum pieces).

Foreign material (aluminum pieces).

Foreign material (aluminum pieces).

Foreign material (aluminum pieces).

Foreign material (aluminum pieces).

Bulk packaged dietary ingredient manufacturer product label does not declare Milk as an allergen ingredient.

Foreign object (glass) found inside sealed container of finished product.

Foreign object (glass) found inside sealed container of finished product.

Failed tablet specifications.

Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract manufacturer.

Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract manufacturer.

Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract manufacturer.

Subpotent Drug

Lack of Assurance of Sterility

Failed Tablet/Capsule Specifications

FOR IMMEDIATE RELEASE – 03/30/2026 - Flushing, New York, Aphreseller (Ebay seller ID), Buy-herbal.com is recalling all lots of Kian Pee Wan capsules to the consumer level. FDA analysis has found that the product contains the undeclared drug ingredients dexamethasone and cyproheptadine. Products cont

The recalled bed rails violate the mandatory standard for adult portable bed rails because users can become entrapped within the bed rail, or between the bed rail and the side of the mattress, posing a serious entrapment hazard and risk of death by asphyxiation. In addition, the bed rails do not bear the required hazard warning labels.