Product may contain egg, an undeclared allergen.
All Recalls
95,075 total recalls in our database
Rajbhog Sweets Jelebi Orange, 9.5 oz packages and sold by weight from bulk trays.
Rajbhog Distributors TX
Undeclared milk
Undeclared Yellow #5
Rajbhog Sweets Jelebi Yellow, 9.5 oz packages and sold by weight from bulk trays.
Rajbhog Distributors TX
Undeclared milk
Gerber Snacks for Baby Soothe 'n' Chew TEETHING STICKS Banana NET WT 3.2 OZ (90g) box UPC 0 15000 04608 8 and NET WT 1.59 oz box UPC 0 15000 01015 7 GERBER PRODUCTS CO., FREMONT, MI 49413
Nestle-USA, Inc. (Corporate Office)
Firm received complaints of infant choking.
Potato flour item #20501 was recalled due to undeclared milk (between 13ppm and 17ppm).
Garden Salad 5 oz Lot # 6620223 Best By: 02.05, UPC 766375733300
FRESHPOINT CENTRAL FLORIDA
Mislabeled salads (undeclared peanut allergen). Incorrect ingredient applied (peanuts)
Gerber Snacks for Baby Soothe 'n' Chew TEETHING STICKS Strawberry Apple NET WT 3.2 OZ (90g) UPC 0 15000 04518 7 GERBER PRODUCTS CO., FREMONT, MI 49413
Nestle-USA, Inc. (Corporate Office)
Firm received complaints of infant choking.
Undeclared Yellow #5
Product may be contaminated with foreign objects (white fragments of plastic, varying in length and width).
Small pieces of plastic broken tray in the product.
Defective Container: Some packets may not be fully sealed, potentially allowing for loss of Ethanol from the product.
Lack of Assurance of Sterility: due to a quality control process deviation. During an internal quality assurance review, an Acceptable Quality Limit (AQL) inspection was not conducted on a statistically sound number of samples. This may result in the inability to assure that the impacted products meet the identity, strength, quality, and purity characteristics that they are purported or represented to possess and may lead to products of unacceptable quality.
ViaMed Alcohol Prep Pads, For External Use Only, 70% Isopropyl Alcohol, Sterile, 100 pieces per Box, 100 boxes per Carton, Sterile, Manufactured by Wuxi Medical Instrument Factory Co., Ltd., Made in China, Manufactured for: Rece International Corp., Miami Lakes, FL, 33014, USA, NDC: 70006-500-01.
Wuxi Medical lnstrument Factory Co.
Lack of assurance of sterility and cGMP deviations observed at the manufacturing site.
Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices
Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices
Error in the IFU lists an incorrect incubation time on one occasion of 20 minutes rather than the correct incubation time of 60 minutes.
Brivo MR355, NMRI system
GE Healthcare (China) Co.
For certain MR systems, a scan can be resumed following a Power Monitor trip when the "6-minute average SAR" is above the limit indicated on the "SAR Display". The user interface may incorrectly enable a scan to proceed earlier than intended. If resumed by the operator, such a scan can result in potential excessive tissue heating, especially if the patient is in contact with a conductive material or has an implant.
Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices
Due to User Manual/Direction for Use incorrectly instructing user to leave the safety clamp in the open position when reloading an infusion set. This issue potentially could result in an accidental over infusion if the roller clamp is left open.