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Safety Reports: Recall

Updated:

Real Time Reports

Recall notice

Aligned Medical Solutions Convenience kits containing saline - recalled due to safety concerns, USA

1 year ago •source fda.gov • details

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

Recalls Aligned Medical Solutions Convenience kits containing saline - recalled due to safety concerns Align... photo #1
312   Comments Comment

Recall notice

Rocket Systems Inc products - recalled due to production without the benefit of inspection, Ohio, USA

1 year ago •source highlandcountypress.com • details

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

#ketogummiesscam #scam #recall #ohio #unitedstates

Recalls Rocket Systems Inc products - recalled due to production without the benefit of inspection Rocket Sy... photo #1
197   Comments Comment

Recall notice

Lubricant Eye Drops & Multi-Symptom Eye Drops - recalled due to potential safety concerns, USA

1 year ago •source fda.gov • details

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

Recalls Lubricant Eye Drops & Multi-Symptom Eye Drops - recalled due to potential safety concerns Kilitch He... photo #1
312   Comments Comment

Recall notice

Pediatrix Acetaminophen Oral Solution - recalled due to potential risk of overdose, Canada

1 year ago •source recalls-rappels.canada.ca • details

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

Recalls Pediatrix Acetaminophen Oral Solution - recalled due to potential risk of overdose Teva Canada Ltd.... photo #1
87   Comments Comment

Recall notice

ELV Alipotec Mexican Tejocte Root Supplement - recalled due to the presence of yellow oleander, USA

2 years ago •source fda.gov • details

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

Recalls ELV Alipotec Mexican Tejocte Root Supplement - recalled due to the presence of yellow oleander WORLD... photo #1
312   Comments Comment

Recall notice

Spring Valley Biotin & Collagen Liquid Natural Berry Flavor Dietary Supplement - recalled due to potential mold contamination, USA

2 years ago •source accessdata.fda.gov • details

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

Recalls Spring Valley Biotin & Collagen Liquid Natural Berry Flavor Dietary Supplement - recalled due to pot... photo #1
313   Comments Comment

Recall notice

Leiters Health Vancomycin, Phenylephrine & Fentanyl IV Bags - recalled due to potential double drug potency, USA

2 years ago •source fda.gov • details

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

Recalls Leiters Health Vancomycin, Phenylephrine & Fentanyl IV Bags - recalled due to potential double drug... photo #1
313   Comments Comment

Recall notice

3-D Pet Products Parrot Food - recalled due to potential Salmonella contamination, Lincoln, Kansas, USA

2 years ago •source fda.gov • details

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

Recalls 3-D Pet Products Parrot Food - recalled due to potential Salmonella contamination Greeley, CO – D&D... photo #1
1   Comments Comment

Recall notice

Atrium Express Drains - recalled due to unverified sterility of provided syringes, USA

2 years ago •source fda.gov • details

Getinge / Atrium Medical Corporation notified affected customers of a nationwide recall (medical device correction) for certain Atrium Express Dry Suction Dry Seal Chest Drains in response to a voluntary medical device recall initiated by a supplier, Nurse Assist. On November 8, 2023, Getinge received notice from… See more

#recall #medicaldevices #unitedstates

Recalls Atrium Express Drains - recalled due to unverified sterility of provided syringes Getinge / Atrium M... photo #1
312   Comments Comment

Recall notice

Blue Ridge Beef Kitten Grind, Kitten Mix, and Puppy Mix Update - recalled due to Salmonella and Listeria, USA

2 years ago •source fda.gov • details

Blue Ridge Beef is expanding their recall to include additional lot numbers due to contamination of Salmonella and Listeria monocytogenes. The products were distributed between 11/14/2023 – 12/20/2023. These products were packaged in clear plastic and sold primarily in retail stores located in the states of: CT,… See more

#recall #animalveterinary #paintlick #kentucky #unitedstates

Recalls Blue Ridge Beef Kitten Grind, Kitten Mix, and Puppy Mix Update - recalled due to Salmonella and List... photo #1
  Comments Comment

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