Nevada recalls

Aju Pharm's AlternatiV+ Max Knotless Anchor surgical device has been recalled due to reports of failure, including anchor breakage, bending, and pulling out during use. The issue affects all lots of models 20KPN4751 and 20KPN5501 distributed in California and Puerto Rico.

Aju Pharm's Genesis Push-In Suture Anchor has been recalled due to reports of device failure during use, including the anchor breaking, bending, or pulling out, as well as suture breakage. About 200 units were distributed nationwide in California and Puerto Rico.

Aju Pharm Co., Ltd. is recalling Genesis Knotless Anchor surgical devices due to reports of device failure. The anchor can break, bend, pull out of tissue, the suture can break, or the packaging can break during handling or use.

Aju Pharm Co., Ltd. is recalling Genesis Dual Thread Screw-In Anchor devices (Models 10N47502 and 10N55002) due to reports of failure during use. The anchor may break, bend, pull out, or cause the suture to break.

Aju Pharm Co., Ltd. is recalling Genesis Screw-In Anchor devices due to reports of failure, including anchor breakage, bending, pull-out, suture breakage, and packaging damage. The recall affects models 10B45003, 10B55003, and 10B65003 distributed nationwide in California and Puerto Rico.

Aju Pharm's Fixone Biocomposite Anchor has been recalled due to reports of device failure, including anchor breakage, bending, pulling out, suture breakage, and packaging damage. The recall affects 1,088 units distributed in California and Puerto Rico. No injuries have been reported to date.

Aju Pharm's Fixone Hybrid Anchor, a surgical device, has been recalled due to reports of device failure. Problems include the anchor breaking, bending, or pulling out during use, as well as suture breakage and packaging damage. This affects 233 units distributed in California and Puerto Rico.

Cerapedics recalled PearMatrix P-15 Peptide Enhanced Bone Graft (1.0cc) due to an incorrect expiration date on certain units. The affected lot is 7014819. No injuries have been reported.

Elekta medical linear accelerators used in cancer radiation therapy have a manufacturing defect affecting electrical grounding in certain models and lot codes. The issue could potentially affect the safe operation of these systems. No injuries have been reported to date.

The Broselow Tape, a tool used in pediatric emergency care to determine medication doses based on a child's length and weight, contains dosing errors for three medications: Vecuronium, Flumazenil, and Ketamine. These errors could lead to incorrect doses being given in emergency situations. The affected units have specific lot numbers and are distributed in the US, Canada, Hong Kong, and Singapore.

The Broselow Tape, a tool used in pediatric emergency care to determine correct medication doses based on a child's length and weight, contains dosing errors for three medications: Vecuronium, Flumazenil, and Ketamine. These errors could lead to incorrect doses being given during emergency treatment.

SunMed Holdings is recalling certain Broselow Pediatric Emergency Rainbow Tapes because they contain incorrect dosing information for three medications: Vecuronium, Flumazenil, and Ketamine. These errors could lead to wrong drug doses during pediatric emergency care. This is a serious safety issue affecting emergency departments and medical facilities.

The Broselow Tape, a tool used in pediatric emergencies to calculate medication doses based on a child's length and weight, contains incorrect dosing information for three medications: Vecuronium, Flumazenil, and Ketamine. These errors could lead to wrong doses being given during emergency care. The FDA has classified this as a Class I recall, the most serious category.

Live it Up brand Super Greens dietary supplement powder may be contaminated with Salmonella Typhimurium. The contamination affects specific lot codes beginning with the letter "A" and expiration dates from August 2026 through January 2028. No illnesses have been reported to date.

Live it Up brand Super Greens dietary supplement powder may be contaminated with Salmonella Typhimurium. The contamination affects specific lot codes beginning with the letter "A" and expiration dates from August 2026 through January 2028. No illnesses have been reported so far.

Prima Vera Nueva's Roasted Green Chile & Jack Cheese Tamales may be contaminated with Listeria monocytogenes, a bacteria that can cause serious illness. The recall affects 24 oz. packages (UPC 748732000034) distributed in California and Nevada.

Prima Vera Nueva Black Bean Bonanza Tamales may be contaminated with Listeria monocytogenes, a bacteria that can cause serious illness. The affected product was distributed in California and Nevada. No illnesses have been reported so far.

Prima Vera Nueva butternut squash tamales with roasted green chiles may be contaminated with Listeria monocytogenes, a bacteria that can cause serious illness. The affected product has UPC 748732000300 and was distributed in California and Nevada.

Prima Vera Nueva roasted green chile tamales may be contaminated with Listeria monocytogenes, a bacteria that can cause serious illness. The affected product is sold in 24 oz packages containing 4 tamales with UPC 748732000270. About 21,705 packages distributed in California and Nevada are involved.

Prima Vera Nueva Black Bean Bonanza Tamales may be contaminated with Listeria monocytogenes, a bacteria that can cause serious illness. The affected product is a 24-ounce package containing 4 tamales with UPC 748732000287. No illnesses have been reported so far.

Prima Vera Nueva is recalling BBQ Chipotle Bean & White Cheddar Tamales because they may be contaminated with Listeria monocytogenes, a bacteria that can cause serious illness. The affected packages were distributed in California and Nevada.

Prima Vera Nueva mushroom, spinach & salsa tamales may be contaminated with Listeria monocytogenes, a bacteria that can cause serious illness. The affected products have UPC 748732000317 and were distributed in California and Nevada. No illnesses have been reported to date.

Prima Vera Nueva roasted pumpkin and white cheddar tamales may be contaminated with Listeria monocytogenes, a bacteria that can cause serious illness. The affected packages were distributed in California and Nevada. No illnesses have been reported to date.

Prima Vera Nueva's Mushroom, Spinach & Salsa Tamales with 2 Cheeses may be contaminated with Listeria monocytogenes, a bacteria that can cause serious illness. The affected product is a 24-ounce package containing 4 tamales (UPC: 748732000249). This recall affects approximately 25,889 packages distributed in California and Nevada.

Prima Vera Nueva butternut squash tamales with roasted green chiles, corn, and jack cheese may be contaminated with Listeria monocytogenes, a bacteria that can cause serious illness. About 30,000 packages were distributed in California and Nevada. No illnesses have been reported so far.

McCafe Premium Roast Decaf Coffee K-Cup Pods may contain caffeine despite being labeled as decaf. This affects 84-count cartons with a Best By date of November 17, 2026, distributed in California, Indiana, and Nevada. No injuries have been reported.

Qunol Extra Strength Turmeric Capsules (1000mg) in 60-count and 120-count bottles have been recalled due to mold contamination in raw materials used to make the product. The contamination was found in material lots produced in July. No injuries have been reported.

Novadoz Pharmaceuticals is recalling specific lots of glycopyrrolate oral solution (1 mg/5 mL) because the medication failed quality testing for impurities and degradation. The affected lots may not meet safety and effectiveness standards. Three lots are involved, with expiration dates between April and May 2027.

Greenstone LLC is recalling methylprednisolone 4 mg Dosepak tablets (Lot #LG7675, expiring November 2026) because the blister foil is oriented incorrectly. This misalignment can make the dosing directions on the foil confusing or unclear, which could lead to taking the wrong dose.

Some bottles of Parodontax Active Gum Health mouthwash (mint, 16.9 FL OZ) may be missing or have illegible lot and expiration date codes. This makes it impossible to know when the product expires. The affected lot is #0665363 with an expiration date of 08/31/2027.