immediate action Recalls

Cipla USA Lanreotide Injection Recall for Sterility Assurance Issue (2026)

Lack of Assurance of Sterility: Due to an FDA observation at the contract manufacturing site for deficiencies in their visual inspection procedure.

Pure Vitamins and Natural Supplements Boner Bears Honey Recall for Undeclared Sildenafil and Tadalaf

FDA analysis revealed the presence of undeclared sildenafil and Tadalafil

Lanreotide Injection recall: Cipla USA lanreotide acetate pre-filled syringes recalled for sterility

Lack of Assurance of Sterility: Due to an FDA observation at the contract manufacturing site for deficiencies in their visual inspection procedure.

Pure Vitamins and Natural Supplements Recall Red Bull Extreme Male Enhancement Supplement for undecl

FDA analysis revealed the presence of undeclared sildenafil

Western Mixers Produce & Nuts Recalls 1 Case Treasured Harvest Chilli Spanish Peanuts (2026)

Foreign object (glass) found inside sealed container of finished product.

Brahms PlGF Plus KRYPTOR 859075N Recall Expands to 5,254 Units Worldwide (2026)

Lidl US Trading Recalled 17,056 Favorina Chocolate Ladybugs for Nut-Labeling Error (2026)

17,056 units of Favorina Chocolate Ladybugs German-Style Nougat from Lidl US Trading are recalled. The recall covers products distributed to DC and 10 states. The label does not specify the type of tree nut contained.

Western Mixers Produce & Nuts Recalls 384 Cases of First Street Chilli Spanish Peanuts Over Glass (H

Foreign object (glass) found inside sealed container of finished product.

Stryker Sustainability Solutions Color Cuff Recall Expands to 56,740 Cuffs Over Detachment Risk (202

Due to potential for tourniquet cuffs to detach from the bladder at the welding connection and result in the cuff not being able to maintain pressure.

17 Stories Furniture Dressers Recalled Over Tip-Over Risk

LIVEHOM Dressers Recalled Over Tip-Over Hazard Risk

LIVEHOM recalled 11-Drawer Dressers on March 12, 2026, due to tip-over hazards. The recall affects dressers sold on Amazon that can pose serious risks to children. Consumers must stop using these dressers immediately and contact the company for a full refund.

LFTE USA Recalls Playground Swing Set Seats Due to Fall Hazard

LFTE USA recalled Playground Swing Set Seats on March 12, 2026. The swing seats pose a fall hazard due to potential rivet failure. The recall affects model number 999604 with the code 'LF-65708' marked on the seat pad.

ProRider Recalls Bicycle Helmets Over Serious Head Injury Risk

ProRider recalled several models of bicycle helmets on March 12, 2026, due to a serious risk of head injury. The helmets do not meet mandatory safety standards and can fail in a crash. Consumers should stop using these helmets immediately and seek a refund.

Stoney Games Recalls Kluster Magnet Chess Games Over Ingestion Risk

Honda Recalls 2023-2025 Pilot and 2023-2024 Passport Over Fuel Tank Filler Leakage (2026)

Honda (American Honda Motor Co.) is recalling certain 2023-2024 Passport and 2023-2025 Pilot vehicles. The fuel filler neck tube and fuel filler pipe may separate, allowing fuel to leak.

Lone Star Dairy Products Recalls 1.79M Lbs Spray Dried Dairy Powder Over Salmonella Risk (2026)

Salmonella spp. identified in finished product testing

Fresenius Kabi 5% Dextrose Injection Recall for Sterility Concerns (2026) Affecting US Nationwide, R

Lack of Assurance of Sterility

Fresenius Kabi 0.9% Sodium Chloride Injection Recalled for Lack of Sterility Assurance (2026)

Lack of Assurance of Sterility

Fresenius Kabi 0.9% Sodium Chloride Injection Recalled for Lack of Sterility Assurance

Fresenius Kabi USA recalls 0.9% Sodium Chloride Injection units distributed nationwide, including Alaska and Puerto Rico. The recall cites lack of assurance of sterility. Healthcare providers should stop use and contact Fresenius Kabi for guidance.

BD and Fresenius Kabi 1,000 mL Sodium Chloride Injection Recall for Sterility Concerns (2026)

Lack of Assurance of Sterility