Moonstruck Chocolate Company The Salty Nutty Toffee Bar, brand ALMA, net weight 1.85 oz recall — FDA F-0750-2019
the Salty Nutty Toffee Bar is recalled due to undeclared soy lecithin
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the Salty Nutty Toffee Bar is recalled due to undeclared soy lecithin
Products recalled due to potential contamination with Listeria monocytogenes or Salmonella.
Shortfill: Aprepitant capsules 40 mg is being recalled due to customer reports of missing capsule in the blister pack.
Subpotent Drug:Out of specification for percentage of active pharmaceutical ingredients.
Failed Impurities/Degradation Specifications:Out of specification for impurities.
Sub-potent
Superpotent Drug: recalled lots may have higher concentration of ibuprofen.
Lack of Sterility Assurance and Incorrect/Undeclared excipient: Product was found to contain undeclared colloidal silver
Subpotent Drug: Isotretinoin content results were lower than the specification limit obtained during routing product monitoring.
Labeling: Not eslewhere classified - The kits include Sodium Chloride, USP, 0.9% which was recalled by the manufacturer due to the product insert incorrectly stating stoppers do not contain…
Defective Container: vial defect was identified that could potentially impact the container closure and result in a lack of sterility assurance and/or the potential for glass particles.
Superpotent Drug: recalled lots may have higher concentration of ibuprofen.
Sub-potent
Labeling: Not eslewhere classified - The kits include Sodium Chloride, USP, 0.9% which was recalled by the manufacturer due to the product insert incorrectly stating stoppers do not contain…
Superpotent Drug: recalled lots may have higher concentration of ibuprofen.
Chrysler (FCA US LLC) is recalling certain 2019 Jeep Cherokee vehicles. The instrument cluster may fail resulting in a lack of activation of warning chimes, messages, and gauges.
Nissan North America, Inc (Nissan) is recalling certain 2019 Altima vehicles. The retainer clip connecting the low pressure fuel tube to the high pressure fuel pump may not have been locked…
Affected lithium-ion batteries may contain a defective component (Thermal Cut-off or TCO). Should the component fail, the battery will no longer charge or deliver power to the…
CIVCO Needle Guide Bracket, REF 674-057-10, Reusable non-sterile bracket for use with FUJIFILM SonoSite, Inc. L25 series tranducers, Rx.
CIVCO Needle Guide Starter Kit, REF numbers P12924-01 and P12924-02, Reusable non-sterile bracket with sterile (1cm, 1.5cm, 2cm depths) needle guides (5), (10.2 x 147cm) CIV-Flex covers (5)…
When your system was installed, the Main disconnect switch, EPO button on the A1 panel, and Remote EPO button(s) (outside of the A1 panel) may not have been wired correctly which could…
The firm has become aware of a potential issue that may affect the mixing motor drive harness and mixing home detection sensor relay harness on your AIA-900 Analyzer. It is possible that…
CIVCO Needle Guide Starter Kit, REF numbers P12920-01 and P12920-02, Reusable non-sterile bracket with sterile (1.5cm, 2.5cm, 3.5cm, 4.5cm depths) needle guides (5), (10.2 x 147cm) CIV-Flex…
The needle guide bracket may puncture the sterile cover applied over the transducer and bracket during assembly.
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