SpecGx Oxycodone Acetaminophen Recall
SpecGx is recalling Oxycodone and Acetaminophen tablets (10 mg / 325 mg) because some tablets may be missing the imprint, making it impossible to verify the …
SpecGx, LLC
Every recall we are tracking for SpecGx, LLC, newest first, sourced from the FDA. If you are wondering whether your SpecGx, LLC product is recalled in 2026, check the list below for your model, lot, or VIN. Each entry explains the hazard and the free repair, replacement, or refund. Get a free email alert the moment a new SpecGx, LLC recall posts.
1 recall · updated Dec 16, 2025
Fresenius Kabi is recalling Naropin (ropivacaine hydrochloride injection) 0.5%, 20 mL single-dose vials because hair was found in some products. Use of …
Fresenius Kabi USA, LLC
Rohto Cooling Eye Drops Max Strength (0.4 FL OZ / 13 mL bottles) has been recalled because the manufacturer cannot confirm the product is sterile. Using …
Rohto-Mentholatum (Vietnam) Co., Ltd.
Rohto Cooling Eye Drops Cool Relief has been recalled because the manufacturer cannot guarantee the product is sterile. Use of non-sterile eye drops can lead to …
Rohto-Mentholatum (Vietnam) Co., Ltd.
Major Pharmaceuticals is recalling Levothyroxine Sodium 88 mcg tablets because they are subpotent, meaning they contain less active ingredient than labeled. …
Major Pharmaceuticals
Major Pharmaceuticals' Levothyroxine Sodium Tablets, USP 75 mcg, have been found to be subpotent, meaning they contain less active ingredient than stated. …
Major Pharmaceuticals
Major Pharmaceuticals is recalling Levothyroxine Sodium Tablets 150 mcg because some batches contain less active ingredient than labeled, which means they may …
Major Pharmaceuticals
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