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Safety Reports: Recall

Updated:

Azurity Pharmaceuticals, Inc. is voluntarily recalling one lot (F230169A) of Zenzedi® CII (dextroamphetamine sulfate tablets, USP) 30 mg to the consumer level. The product is being recalled due to a report from a pharmacist in Nebraska who opened a bottle of Zenzedi® 30 mg tablets and found… See more

#recall #drugs #unitedstates

Haleon is voluntarily recalling eight lots of Robitussin Honey CF Max Day Adult and Robitussin Honey CF Max Nighttime Adult to the consumer level. The product is being recalled due to microbial contamination. To date, Haleon has not received any reports of adverse events related to this… See more

#recall #drugs #unitedstates

Aligned Medical Solutions, initiated a nationwide recall of Convenience kits containing saline because the Product cannot be verified as having the required sterility assurance level. Product(s) can be identified by the pack label inside the sterile barrier of the convenience kit. Aligned Medical Solutions distributed these kits… See more

#recall #medicaldevices #unitedstates

Rocket Systems Inc. is voluntarily recalling various of its products, including the ACV Gummy, CBD Gummy, CBD Tincture, Capsule products, and cosmetics. The recall comes due to a lack of inspections from the Ohio Department of Agriculture. There haven't been any reports of sickness linked to these… See more

#recall #ohio #unitedstates

Kilitch Healthcare India Limited is issuing an amendment in the last Nationwide press release dated November 13, 2023 issued for nationwide recall of various eye drops. These products were distributed nationwide in the USA to wholesalers, retailers, and via the product distributor, Velocity Pharma LLC.

There are… See more

#recall #drugs #unitedstates

Teva Canada Ltd. is recalling a single lot of its Pediatrix Acetaminophen Oral Solution for children due to an increased risk of overdose. The product was distributed nationwide in Canada. The product is available without a prescription and is used to relieve mild to moderate pain and… See more

#drugs #recall #canada

WORLD GREEN NUTRITION, INC. is recalling ELV ALIPOTEC brand MEXICAN TEJOCOTE ROOT SUPPLEMENT PIECES (RAIZ DE TEJOCOTE MEXICANO SUPLEMENTO EN TROZOS), NET. WT, 0.3 0Z (7g), due to the presence of yellow oleander in this product. The consumption of yellow oleander can cause adverse effects on neurological,… See more

#recall #unitedstates

FDA announced the recall of 24,324 units of Spring Valley Biotin & Collagen Liquid Natural Berry Flavor Dietary Supplement by BioMylz Pvt. Ltd. due to potential mold contamination. This product was distributed to a distribution center in California and then further distributed to distribution centers and retail… See more

#dietarysupplements #recall #unitedstates

Leiters Health is voluntarily recalling 33 lots of products to the user level. The recalled batches of vancomycin IV bags, phenylephrine IV bags, and fentanyl IV bags are being recalled due to the potential for superpotency because they may contain twice the labeled amount of drug. The… See more

#recall #drugs #unitedstates

Greeley, CO – D&D Commodities Ltd. is voluntarily recalling one lot of 3-D® Pet Products Premium Parrot Food, due to potential Salmonella contamination. The affected parrot food product is packaged in clear plastic jars and was distributed to retailers and distributors in the following states: Arizona, Arkansas,… See more

#recall #petfood #lincoln #kansas #unitedstates