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All product recalls associated with Damon Industries.
Total Recalls
275
Past Year
5
Class I (Serious)
17
Most Recent
Dec 2025
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
Firm discovered that Worcestershire sauce used in making various drink mixes contains anchovies which were not declared on the ingredient label or Allergan information.
Firm discovered that Worcestershire sauce used in making various drink mixes contains anchovies which were not declared on the ingredient label or Allergan information.
Firm discovered that Worcestershire sauce used in making various drink mixes contains anchovies which were not declared on the ingredient label or Allergan information.
Firm discovered that Worcestershire sauce used in making various drink mixes contains anchovies which were not declared on the ingredient label or Allergan information.
Firm discovered that Worcestershire sauce used in making various drink mixes contains anchovies which were not declared on the ingredient label or Allergan information.
Firm discovered that Worcestershire sauce used in making various drink mixes contains anchovies which were not declared on the ingredient label or Allergan information.
Firm discovered that Worcestershire sauce used in making various drink mixes contains anchovies which were not declared on the ingredient label or Allergan information.
The retaining tabs component of the Set Screw Retaining Drive may be oversized, which will not allow proper mating between the Set Screw Retaining Drive and the set screw.
AMO has received complaints where the finger grip dislodged while depressing the syringe plunger. The finger grip dislodgement could result in the surgeon's hand unintentionally moving the cannula further than intended, resulting in potential trauma to the eye.
Diamond Coach Corporation (Diamond) is recalling certain model year 2006-2011 VIP and PT 2000, 2200, 2500, 2800, 3200, and 3201 transit buses manufactured January 1, 2006, to December 31, 2011, equipped with certain model S2005, S2010, S5005, S5010, S5505, and S5510 wheelchair lifts manufactured by Ricon Corporation. The platform side plate of the affected wheelchair lifts may crack.
Gluten Protein detected up to 50 ppm in product with gluten free statement.
Undeclared Allergen: Egg
This recall involves all Paramount Trident Series 2 (UV II) ultraviolet sanitation systems. The sanitation systems are a gray tube that stands 32 inches high by 11 inches in diameter. They are plumbed into the pool's water circulation pipes and plugged in or hard-wired into an electrical system. The pool's water runs through the unit and is sanitized by ultraviolet lamps. This is a secondary sanitation system used in conjunction with chemical sanitizers such as chlorine or bromine. "Trident UV II" or "Series 2 Trident Ultraviolet Corporation UV Sanitation System" is printed on a black label on the front of the units. In addition, a silver sticker on the units has the following wording "Paramount Series 2 Ultraviolet Pool Sanitizer System," "Trident Series 2 Ultraviolet Water Treatment System" or "Trident Ultra UV Series 2 Water Treatment System" and a date code of 9/9/2013 or later. Some date codes consist of a series of letters. Consumers with letters in the date code need to go to www.1paramount.com to determine if their unit is included in the recall.
Kettle Foods, Inc. is recalling Bakes Sea Salt Potato Chips, Kettle Brand, due to potential undeclared milk.
The firm initiated this recall in response to FDA sample findings that major ingredients are omitted partially or entirely. The product did not contain the amounts as labeled for Vitamin A and Vitamin C.
Marketed Without an Approved NDA/ANDA; products have been found to contain tadalafil, the active ingredient in an FDA approved product used to treat erectile dysfunction, making this product an unapproved drug
Marketed Without an Approved NDA/ANDA; products have been found to contain tadalafil, the active ingredient in an FDA approved product used to treat erectile dysfunction, making this product an unapproved drug
DIAMOND COACH CORPORATION (DIAMOND COACH) IS RECALLING CERTAIN MODEL YEAR 2008-2010 PT AND VIP BUSES EQUIPPED WITH BRAUN CENTURY-2 AND VISTA-2 WHEELCHAIR LIFTS. OVER TIME, AND WITH FREQUENT USE, THE ROLL STOP LATCHES ON THE WHEELCHAIR LIFTS OUTER BARRIER MAY BECOME BENT OR MISALIGNED.
Molluscan shellfish may have been exposed to human fecal waste and are potentially contaminated with norovirus.
HARLEY DAVIDSON IS RECALLING ACCESSORY BRAKE LINE KITS SOLD FOR INSTALLATION ON CERTAIN MODEL YEAR 1996-2012 DYNA AND CERTAIN MODEL YEAR 1999-2012 SOFTAIL MOTORCYCLES. DUE TO MANUFACTURING AND INSTALLATION CONDITIONS THESE ACCESSORY BRAKE LINE KITS MAY LEAK.