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Safety Reports: Recall

Updated:

TYSON Tonic Kava & Kratom Blend shots - recalled due to unapproved food additive: kratom, USA

11 months ago •source accessdata.fda.gov • details

Recall notice

FDA announced the recall of 15,000 units of TYSON Tonic Kava & Kratom Blend shots by LGNDS LLC because the products contain kratom (an unapproved food additive) and pH is over 5.0. The process authority letter classified product as acidified and pH cannot exceed 3.30. These products… See more

#supplement #recall #unitedstates

TYSON Tonic Kava & Kratom Blend shots - recalled due to unapproved food additive: kratom photo #1
312

Garden of Life whole Food Dietary Supplements - recalle due to undeclared soy, USA

11 months ago •source accessdata.fda.gov • details

Recall notice

FDA announced the recall of Garden of Life whole Food Dietary Supplements by Garden Of Life Llc due to undeclared Soy. These products were distributed in the US.

The recalled products are:
- Garden of Life, FYI ULTRA, ULTIMATE Joint & Cartilage Formula, Whole Food Dietary Supplement,… See more

#recall #supplement #unitedstates

Garden of Life whole Food Dietary Supplements - recalle due to undeclared soy photo #1
314

InvaGen Pharmaceuticals Inc. Vigabatrin for Oral Solution - recalled due to malfunction, USA

11 months ago •source fda.gov • details

Recall notice

Cipla Limited today announced that its wholly-owned subsidiary, InvaGen Pharmaceuticals Inc. is voluntarily recalling one lot of Vigabatrin for Oral Solution, USP 500mg, to the consumer level. Vigabatrin for Oral Solution, USP 500 mg has been found to have seal integrity issues allowing for powder leakage from… See more

#recall #drugs #unitedstates

InvaGen Pharmaceuticals Inc. Vigabatrin for Oral Solution - recalled due to malfunction photo #1
312

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

11 months ago •source fsai.ie • details

Recall notice

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

Artri King, Kuka Flex Forte and Reumo Flex food supplements - recalled due to not permitted active ingredients photo #1
19

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

11 months ago •source fda.gov • details

Recall notice

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

Kodiak Premium Wintergreen Longcut Smokeless Tobacco - recalled due to the presence of foreign metal objects photo #1

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

11 months ago •source fda.gov • details

Recall notice

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

#medicaldevices #recall #unitedstates

Covidien and Cardinal Health Urology and OR room specific kits and trays - recalled due to lack of sterility assurance photo #1
312

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

11 months ago •source fda.gov • details

Recall notice

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

Baxter Novum IQ syringe infusion pump - recalled due to malfunction photo #1
312

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

11 months ago •source fda.gov • details

Recall notice

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

Magnum Male Sexual Enhancement capsule - recalled due to undeclared sildenafil photo #1
312

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

1 year ago •source fda.gov • details

Recall notice

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

Novartis Sandimmune Oral Solution - recalled due to due to crystallization formation photo #1
312

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

1 year ago •source fda.gov • details

Recall notice

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

TING® 2% Miconazole Nitrate Athlete’s Foot Spray Antifungal SprayPowder - recalled due to the presence of benzene photo #1
313

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