Massachusetts recalls

Taro Pharmaceuticals is recalling one lot of fluocinonide 0.05% cream due to viscosity testing that showed the cream is thicker than the approved specification. This may affect how the medication spreads and absorbs. No injuries have been reported.

Taro Pharmaceuticals is recalling Fluocinonide 0.05% Cream (30g tubes, Lot AD76251, expiring 6/30/2026) because the product's thickness is outside the acceptable range. This was discovered during stability testing. The thicker-than-normal cream may affect how well it spreads and works on skin.

Taro Pharmaceuticals is recalling one lot of fluocinonide 0.05% cream due to a manufacturing defect. Testing found the cream's thickness was thicker than specifications allow, which could affect how the medication works on your skin.

The FDA inspected the manufacturing facility for QC Quality Choice menthol cough drops on August 15, 2025, and found observations that may affect product quality. The company is recalling one lot of vanilla honey flavor cough drops sold nationwide.

QC Quality Choice menthol cough drops are being recalled because the FDA found quality concerns during an inspection of the manufacturing facility on August 15, 2025. The recall affects specific lot numbers with expiration dates in May and July 2026. No injuries have been reported.

QC Quality Choice Menthol-Cough Suppressant Oral Anesthetic Cough Drops in Honey Lemon flavor are being recalled because the FDA found quality concerns during an inspection of the manufacturing facility in August 2025. The affected product is the 30-count bag with lot number 20240720 and expiration date 07/20/2026.

QC Quality Choice Pectin Oral Demulcent Throat Soothing Drops (Creamy Strawberry, 30-count) are being recalled due to manufacturing quality issues found during an FDA inspection. The recall affects lot #20240720 with an expiration date of 07/20/2026, distributed nationwide.

The FDA inspected the manufacturing facility for QC Quality Choice Menthol-Cough Suppressant Oral Anesthetic Cough Drops on August 15, 2025, and identified quality concerns. The recall affects specific lots distributed nationwide. No injuries have been reported.

The FDA inspected the manufacturing facility for QC Quality Choice menthol cough drops on August 15, 2025, and found quality concerns. The company is recalling cherry-flavored cough drops from two specific production batches out of an abundance of caution.

QC Quality Choice menthol cough drops (black cherry flavor, sugar free) are being recalled because the FDA found quality control issues during a factory inspection on August 15, 2025. The specific concern affects lot #20240720 with expiration date 07/20/2026. No injuries have been reported.

MGC Health Menthol Cough Drops (Honey Lemon flavor, 80-count bags) are being recalled because the FDA found quality concerns during an inspection of the manufacturing facility on August 15, 2025. The recall affects lot #20240730 with an expiration date of July 30, 2026, distributed nationwide.

MGC Health Menthol Cough Drops (Honey Lemon flavor, 30-count bags) are being recalled after the FDA found quality concerns during an inspection of the manufacturing facility on August 15, 2025. The recall affects products with lot number 20240524 and expiration date 05/24/2026 distributed nationwide.

The FDA recommended a recall of MGC Health Menthol Cough Drops (Sugar Free, Honey Lemon) after inspecting the manufacturing facility on August 15, 2025, and identifying quality control issues. The recall affects three specific product lots distributed nationwide.

The FDA inspected the manufacturing facility for these cough drops on August 15, 2025, and found observations that may affect product quality. The affected product is a 30-count bag of Discount Drug Mart menthol cough drops (Lot #20241030, expiring 10/30/2026) distributed nationwide.

The FDA inspected the manufacturing facility for these honey lemon menthol cough drops on August 15, 2025, and found observations that may affect product quality. The affected product is a 30-count bag with lot number 20241030 and expiration date 10/30/2026, distributed nationwide.

The FDA inspected the manufacturing facility for Caring Mill menthol cough drops on August 15, 2025, and found observations that raised concerns about product quality. The manufacturer is recalling the product out of caution. No injuries have been reported.

The FDA recommended a recall of Exchange Select menthol cough drops after inspecting the manufacturing facility in China on August 15, 2025, and finding observations that may affect product quality. The affected product is a 30-count bag with lot number 20241030 and expiration date 10/30/2026.

The FDA found quality concerns at the manufacturing facility during an inspection on August 15, 2025. Exchange Select menthol cough drops (30-count bags, lot #20241030, expiring 10/30/2026) sold at military exchanges may be affected. No injuries have been reported.

SLMD Benzoyl Peroxide Acne Lotion 2.5% in 0.7 fl. oz and 1.5 fl. oz bottles has been found to contain benzene, a chemical that should not be present in this product. This affects approximately 2,500 bottles distributed nationwide. No injuries have been reported.

Sandra Lee MD's SLMD BP Acne Spot Treatment (10% Benzoyl Peroxide) has been recalled because it contains benzene, a harmful chemical. The affected product is sold in 0.5 fl. oz bottles with lot numbers 2567200 (expires 8/1/26) or 2691600 (expires 10/30/2027). No injuries have been reported.

HydroPeptide Clear Alliance Serum (2.5% benzoyl peroxide) contains benzene, a harmful chemical not intended in the product. The affected bottles are 1 FL OZ and 2 FL OZ sizes with lot numbers 2518800 and 2518900. No injuries have been reported, but the FDA has issued a recall due to potential health risks from benzene exposure.

FarmHouse Fresh Midnight Clearing night lotion (2.5% benzoyl peroxide) contains benzene, a harmful chemical not meant to be in this product. The contamination was found in three specific lot numbers. No injuries have been reported so far.

Cipla USA is recalling certain batches of cinacalcet 90 mg tablets because they contain higher-than-safe levels of a chemical impurity called N-Nitroso Cinacalcet. The affected bottles were distributed nationwide. No injuries have been reported.

Cipla USA is recalling specific lots of Cinacalcet Hydrochloride 60 mg tablets because they contain higher-than-acceptable levels of N-Nitroso Cinacalcet, a nitrosamine impurity. This impurity can pose a health risk with long-term exposure. The affected lots were distributed nationwide.

Cipla USA is recalling specific lots of Cinacalcet Hydrochloride 30 mg tablets because they contain higher-than-acceptable levels of a chemical impurity called N-Nitroso Cinacalcet. The affected tablets were distributed nationwide. This is a manufacturing quality issue; no injuries have been reported.

Revival Animal Health is recalling Breeder's Edge® Foster Care® and Shelter's Choice® Canine Milk Replacers because some batches contain unsafe vitamin D levels—either too low or too high. Dogs eating products with high vitamin D may develop serious health problems including kidney disease.

JC Sales recalled Lil' Buddies Pet Laser Toys (model 24496) because they contain button cell batteries that can be swallowed by young children, posing a serious injury or death risk. The toys—white with small blue paw prints—also have tentacle ends that can choke small children and violate safety standards for children's toys. No injuries have been reported yet.

SpringFlower 5-in-1 Montessori Toy Sets sold on Amazon contain an airplane-shaped teething toy with tentacles that can detach and pose a choking risk to young children. The toy also violates safety standards for teething toys. About 21,900 sets were sold from October 2023 through November 2025.

Apex Gaming PCs is recalling ATX computer power supplies under both the Apex and Manik brand names because they lack a permanent warning label about electrical shock hazards. If opened or taken apart, these units can cause serious injury or death from electrocution. The recall affects 450W, 750W, 1000W, and 1200W models sold online from December 2021 through February 2026.

Zoliquex portable bed rails can trap users between the rail and mattress, creating a serious risk of injury or death by asphyxiation. The rails also lack required warning labels. About 16,000 units were sold on Amazon between August 2023 and February 2026.