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Safety Reports: Recall

Updated:

Real Time Reports

Recall notice

Artri King, Kuka Flex Forte and Reumo Flex food supplements - recalled due to not permitted active ingredients, Ireland

2 years ago •source fsai.ie • details

The FSAI announced the recall of Artri King, Kuka Flex Forte, and Reumo Flex food supplements because they contain active ingredients not approved for use in food products and are not declared on the label. All three products contain the active ingredient diclofenac and Artri King also… See more

#recall #ireland

Recalls Artri King, Kuka Flex Forte and Reumo Flex food supplements - recalled due to not permitted active i... photo #1
19   Comments Comment

Recall notice

Kodiak Premium Wintergreen Longcut Smokeless Tobacco - recalled due to the presence of foreign metal objects, Alton, Kentucky 40342, USA

2 years ago •source fda.gov • details

American Snuff Company (ASC) is voluntarily recalling certain lots of Kodiak Premium Wintergreen Longcut Tobacco manufactured at ASCs facility in Clarksville, TN. ASC initiated the recall of Kodiak Premium Wintergreen Longcut Tobacco after having identified the potential for certain lots of the product to contain foreign metal… See more

#recall #tobacco #alton #kentucky #unitedstates

Recalls Kodiak Premium Wintergreen Longcut Smokeless Tobacco - recalled due to the presence of foreign metal... photo #1
  Comments Comment

Recall notice

Covidien and Cardinal Health Urology and OR room specific kits and trays - recalled due to lack of sterility assurance, USA

2 years ago •source fda.gov • details

In direct response to the Nurse Assist, LLC voluntary product recall (which included products supplied to Cardinal Health used in Covidien and Cardinal Health™ brand kits and trays), Cardinal Health issued a medical device recall on December 5, 2023, for its Covidien and Cardinal Health™ brand urology… See more

#recall #medicaldevices #unitedstates

Recalls Covidien and Cardinal Health Urology and OR room specific kits and trays - recalled due to lack of s... photo #1
312   Comments Comment

Recall notice

Baxter Novum IQ syringe infusion pump - recalled due to malfunction, USA

2 years ago •source fda.gov • details

Baxter International Inc. announced today it has issued an Urgent Medical Device Correction for the Novum IQ syringe infusion pump. The Correction is due to the potential for an incomplete infusion following one or more downstream occlusion alarms. Baxter notified impacted customers in October and is developing… See more

#recall #medicaldevices #unitedstates

Recalls Baxter Novum IQ syringe infusion pump - recalled due to malfunction Baxter International Inc. announ... photo #1
312   Comments Comment

Recall notice

Magnum Male Sexual Enhancement capsule - recalled due to undeclared sildenafil, USA

2 years ago •source fda.gov • details

Meta Herbal is voluntarily recalling 500 blister packs of Magnum XXL 9800 2000 mg per capsule, to the consumer level. The products have been found to be tainted with Sildenafil. Products containing sildenafil cannot be marketed as dietary supplements. Magnum XXL 9800 capsules is an unapproved new… See more

#drugs #recall #amazon #unitedstates

Recalls Magnum Male Sexual Enhancement capsule - recalled due to undeclared sildenafil Meta Herbal is volun... photo #1
312   Comments Comment

Recall notice

Novartis Sandimmune Oral Solution - recalled due to due to crystallization formation, USA

2 years ago •source fda.gov • details

Novartis is conducting a voluntary nationwide recall at the consumer level of two lots of its Sandimmune® Oral Solution (cyclosporine oral solution, USP), 100 mg/mL in the US due to crystal formation observed in some bottles, which could potentially result in incorrect dosing. The issue was identified… See more

#recall #drugs #unitedstates

Recalls Novartis Sandimmune Oral Solution - recalled due to due to crystallization formation Novartis is con... photo #1
312   Comments Comment

Recall notice

TING® 2% Miconazole Nitrate Athlete's Foot Spray Antifungal SprayPowder - recalled due to the presence of benzene, USA

2 years ago •source fda.gov • details

Insight Pharmaceuticals, a Prestige Consumer Healthcare Inc. company ("Insight"), is voluntarily recalling two lots of TING® 2% Miconazole Nitrate Athlete's Foot Spray Antifungal Spray Powder to the consumer level. A recent review by our manufacturer and their third-party lab found that samples from two lots of the… See more

#recall #drugs #unitedstates

Recalls TING® 2% Miconazole Nitrate Athlete’s Foot Spray Antifungal SprayPowder - recalled due to the presen... photo #1
313   Comments Comment

Recall notice

Bayer Vitrakvi (larotrectinib) Oral Solution - recalled due to microbial contamination, USA

2 years ago •source fda.gov • details

Bayer is voluntarily recalling one lot of Vitrakvi® (larotrectinib) Oral Solution 20 mg/mL in 100mL glass bottles to the consumer/user level. The product is being recalled due to microbial contamination identified as Penicillium brevicompactum observed during routine ongoing stability testing. It was distributed to wholesale distributors and… See more

#recall #drugs #unitedstates

Recalls Bayer Vitrakvi (larotrectinib) Oral Solution - recalled due to microbial contamination Bayer is volu... photo #1
312   Comments Comment

Recall notice

Noah's Wholesale, LLC Dietary Supplement - recalled due to undeclared Sildenafil, USA

2 years ago •source fda.gov • details

Noah's Wholesale, LLC is voluntarily recalling one lot of rock# 03032021, exp:12/2027, 1200 mg/capsule, to the consumer level. FDA analysis has found the product to be tainted with Sildenafil. The product was distributed locally through convenience stores and some island jobbers (small wholesale distributors to retail). Noah's… See more

#vitamins #recall #drugs #unitedstates

Recalls Noah’s Wholesale, LLC Dietary Supplement - recalled due to undeclared Sildenafil Noah’s Wholesale,... photo #1
312   Comments Comment

Recall notice

KinderMed OTC Pain and Fever Reliever for Infants and Kids - recalled due to Acetaminophen Instability, USA

2 years ago •source fda.gov • details

KinderFarms, LLC is voluntarily recalling all lots of KinderMed Infants' Pain & Fever (oral suspension) and KinderMed Kids' Pain & Fever (oral suspension) to the retail and consumer level. These products are being voluntarily recalled due to acetaminophen instability. These products are available nationwide in drug/pharmacy, supermarkets,… See more

#recall #drugs #unitedstates

Recalls KinderMed OTC Pain and Fever Reliever for Infants and Kids - recalled due to Acetaminophen Instabili... photo #1
312   Comments Comment

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