Tag: medwatch

Par Health Recalls Two Lots of Brevital Sodium Over Cellulose Particulate Matter

14 Oct 2026 4:46 p.m.

The nationwide recall of Brevital Sodium 500 mg/vial, distributed to wholesalers between July 2025 and May 2026, carries a risk of life-threatening adverse health consequences including pulmonary emboli.

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Par Health Recalls 22 Lots of Argatroban Injection Nationwide Over Particulate Matter

14 Oct 2026 4:56 p.m.

The voluntary recall to the hospital/user level covers lots distributed nationwide between December 30, 2024, and May 5, 2026, after cellulose, polystyrene, polyethylene terephthalate, stopper material and possibly stainless steel were detected in certain lots.

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Leader Formulas Recalls RAPTURE Preworkout Nationwide Over DMAA

8 Oct 2026 9:46 a.m.

The Tomball, Texas, company is voluntarily recalling one lot of the supplement powder after FDA testing found DMAA, which can raise blood pressure and cause cardiovascular problems.

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Pacific Health Sciences Recalls One Lot of Babies' Magic Tea Baby Sleep Gripe Water Over Undeclared Alcohols

8 Oct 2026 9:06 a.m.

FDA testing found undeclared ethanol, methanol and isopropanol in Lot 25122bw, and parents and caregivers are told to stop using it.

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Greenwich Rx Recalls Compounded Glutathione Nationwide Over Elevated Endotoxin Levels

2 Oct 2026 8:05 a.m. · Source: US Food and Drug Administration

Greenwich Rx is recalling specific lots of compounded glutathione nationwide after two patients needed emergency care following IV use of a product not formulated for IV administration.

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Global Mix Recalls Niwali Tejocote Capsules and Pieces Over Yellow Oleander Contamination

22 Sep 2026 7:59 a.m. · Source: US Food and Drug Administration

Global Mix recalls niwali Tejocote Capsules and Pieces nationwide after FDA found the products appear to be toxic yellow oleander, which can cause severe or fatal health effects.

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Par Health Recalls Two Lots of Dexmedetomidine Injection Over Particulate Matter

22 Sep 2026 7:53 a.m. · Source: US Food and Drug Administration

Par Health is recalling two lots of Dexmedetomidine HCl in 0.9% Sodium Chloride Injection to the hospital level after cellulose or stopper material was found in the product.

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Otsuka ICU Medical Recalls Sodium Chloride Injection Lot Over Potassium Chloride Mix-Up

22 Sep 2026 7:49 a.m. · Source: US Food and Drug Administration

Otsuka ICU Medical recalls one lot of 0.9% Sodium Chloride Injection after a customer found a highly concentrated Potassium Chloride bag inside the overwrap, warning of potentially fatal outcomes.

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A&P Creations Recalls X10 Natural Enhancement Supplement Over Undeclared Viagra and Cialis Ingredients

16 Sep 2026 7:15 a.m. · Source: US Food and Drug Administration

A&P Creations is recalling X10 Natural Enhancement Supplement after undeclared sildenafil and tadalafil were found in the product, which was sold nationwide through Amazon, Walmart.com and naturefuel.us.

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Q’Apel Medical Recalls and Discontinues 072 Aspiration System (Hippo)

24 Apr 2025 10:23 a.m. · Source: US Food and Drug Administration

Q’Apel Medical Inc. recalls 1,617 units of its 072 Aspiration System (Hippo) due to concerns about the distal tip design. The company has chosen to discontinue the product line.

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