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Consumer Product Recalls

127,244 recalls from the U.S. Consumer Product Safety Commission, newest first.

March 11, 2026Food & BeverageFDA
Bader Enterprises, Inc. recalls Premium Food Bubble Gum, packed in 2.5 oz clear flexible plastic packaging, all lots and codes. Sold in unit case of 30
Hazard: Contains undeclared colors (FD&C Blue 1 Lake and FD&C Blue 2 Lake).
March 11, 2026Food & BeverageFDA
Bader Enterprises, Inc. recalls Premium Food Jordan Almonds, packed in 2.0 oz and 3.5 oz clear flexible plastic packaging.
Hazard: Contains undeclared allergen (wheat) and colors (FD&C Blue 1 Lake and FD&C Blue 2 Lake).
March 11, 2026DrugsFDA
MYLAN PHARMACEUTICALS INC recalls Amnesteem (Isotretinoin) Capsules, USP 40 mg, packaged in 3 x 10-Count Prescription Packs, Rx Only, Manufactured for: My
Hazard: Failed Dissolution Specifications
March 11, 2026DrugsFDA
StuffbyNainax recalls MR. 7 SUPER 700000 capsules, 1 capsule blister card, Distributed by mR. 7
Hazard: Marketed Without an Approved NDA/ANDA: FDA analysis revealed the presence of undeclared sildenafil and tadalafil
March 11, 2026DrugsFDA
Mohamed Hagar recalls Mojo Max Fusion XXX, 500 mg, one capsule per blister card, 20 count box, Distributed by: Max Nutrition Inc. UPC 6 78945
Hazard: Marketed Without an Approved NDA/ANDA-FDA analysis revealed undeclared sildenafil (13.1 mg/capsule) and tadalafil (13.8 mg/capsule).
March 11, 2026DrugsFDA
New Life Pharma LLC recalls Tirzepatide Inj, 15mg x 4, Sterile Multi-Dose Vial, Rx only, Nomida, 25055 W Valley Pkwy, Suite 106, Olathe, KS 66061, N
Hazard: Lack of Assurance of Sterility
March 11, 2026DrugsFDA
New Life Pharma LLC recalls Tirzepatide Inj, 10mg, Sterile Multi-Dose Vial, Rx only, Nomida, 25055 W Valley Pkwy, Suite 106, Olathe, KS 66061, NDC 8
Hazard: Lack of Assurance of Sterility
March 11, 2026DrugsFDA
New Life Pharma LLC recalls Semaglutide Inj., 2 mg x 5, Sterile Multi-Dose Vial, Rx only, Nomida, 25055 W Valley Pkwy, Suite 106, Olathe, KS 66061,
Hazard: Lack of Assurance of Sterility
March 11, 2026DrugsFDA
New Life Pharma LLC recalls Semaglutide Inj, 2mg x 10, Sterile Multi-Dose Vial, Rx only, Nomida, 25055 W Valley Pkwy, Suite 106, Olathe, KS 66061, N
Hazard: Lack of Assurance of Sterility
March 11, 2026DrugsFDA
Radnostix recalls Sodium Iodide (I-131) Solution, Therapeutic Oral, packaged as a) 1 ml V-vial, NDC 69208-003-15; Order 49317, 49323, 4932
Hazard: Presence of Particulate Matter: Due to production issues
March 11, 2026DrugsFDA
ANTHONY TRINH, 123Herbals LLC recalls SILINTAN 25/pills, packaged in a 25-count bottle, Shanghai Chinese Medical Works, Shanghai, China
Hazard: Marketed Without an Approved NDA/ANDA: FDA analysis revealed the presence of undeclared meloxicam.
March 11, 2026DrugsFDA
HTO Nevada Inc. dba Kirkman recalls MAXIMUM, ZONE 2, 4% Lidocaine Cream, (Lidocaine 4% and Epinephrine 0.01%), 1 oz bottles, Distributed By: Dermal Source,
Hazard: Stability Data Does Not Support Expiry Date.
March 11, 2026DrugsFDA
HTO Nevada Inc. dba Kirkman recalls MAXIMUM, ZONE 1, 4% Lidocaine Cream, 1/2 oz bottles, Distributed By: Dermal Source, Portland, OR 97232, NDC 80069-014.
Hazard: Stability Data Does Not Support Expiry Date.
March 11, 2026DrugsFDA
HTO Nevada Inc. dba Kirkman recalls FIVE-STAR, VASOCAINE Spray, (Lidocaine HCl 4%, Racepinephrine HCl 0.01%), 4oz bottles, Distributed By: Dermal Source, Po
Hazard: Stability Data Does Not Support Expiry Date.
March 11, 2026DrugsFDA
Rising Pharma Holding, Inc. recalls Product label: Temozolomide Capsules, 5mg, packaged in 5-capsule bottles, Rx only, Manufactured for: Rising Pharmaceutic
Hazard: Failed Impurities/Degradation Specifications: An out-of-specification result observed during 9th-month long term stability testing
March 11, 2026DrugsFDA
The Harvard Drug Group LLC recalls Midodrine Hydrochloride Tablets, USP, 5 mg, 50 Tablets (5 x 10 blister packs), Rx only, Packaged and Distributed by: Maj
Hazard: Defective container; inadequately sealed blister packaging.
March 11, 2026DrugsFDA
Cipla USA, Inc. recalls Nilotinib Capsules, 200 mg per capsule, packaged in cartons, Rx only, Manufactured for: Cipla USA, Inc., 10 Independence
Hazard: Failed Tablet/Capsule Specifications: Observed OOS results at 6-months long-term stability condition for Description test and Appearance by Visual Inspection test.
March 11, 2026DrugsFDA
Cipla USA, Inc. recalls Nilotinib Capsules, 150 mg per capsule, packaged in cartons, Rx only, Manufactured by: Cipla Ltd., Verna, Goa, India, Ma
Hazard: Failed Tablet/Capsule Specifications: Observed OOS results at 6-months long-term stability condition for Description test and Appearance by Visual Inspection test.
March 11, 2026DrugsFDA
Harbin Jixianglong Biotech Co., Ltd. recalls Semaglutide, For Rx compounding use only, packaged in a) 1g, NDC 84385-106-01; b) 5g, NDC 84385-106-02; c) 10g, NDC 843
Hazard: CGMP Deviations This recall has been initiated due to failing to complete process validation and bacterial endotoxin method validation before distribution
March 11, 2026DrugsFDA
Harbin Jixianglong Biotech Co., Ltd. recalls Semaglutide, For Rx compounding use only, packaged in a) 1g, NDC 84385-106-01; b) 5g, NDC 84385-106-02; c) 10g, NDC 8438
Hazard: CGMP Deviations This recall has been initiated due to failing to complete process validation and bacterial endotoxin method validation before distribution
March 11, 2026DrugsFDA
ACME UNITED CORPORATION recalls Antimicrobial Alcohol Hand Wipe, Isopropyl Alcohol 70%, Manufactured for : Custom Packaging Co., Inc, Louisville, KY 402
Hazard: CGMP Deviations
March 11, 2026DrugsFDA
ACME UNITED CORPORATION recalls Children's Healthcare of Atlanta, Instant Hand Sanitizing Wipe(Benzalkonium Chloride 0.13%), 1000 per case, Made in USA
Hazard: CGMP Deviations
March 11, 2026DrugsFDA
ACME UNITED CORPORATION recalls Dynarex, BZK Antiseptic Towelettes (Benzalkonium Chloride 0.13%), 5x7, 1000 packets, 5x7, Manufactured for Dynarex Corpo
Hazard: CGMP Deviations
March 11, 2026DrugsFDA
ACME UNITED CORPORATION recalls Dynarex, BZK Antiseptic Towelettes (Benzalkonium Chloride 0.13%), 100 packets, 5x7, Manufactured for Dynarex Corporation
Hazard: CGMP Deviations
March 11, 2026DrugsFDA
ACME UNITED CORPORATION recalls Green Guard Antiseptic Wipes (Benzalkonium Chloride 0.13%), 25 wipes per box, Distributed by Green Guard, St. Louis, MO
Hazard: CGMP Deviations
March 11, 2026DrugsFDA
ACME UNITED CORPORATION recalls Hand Sanitizing Wipes (Benzalkonium Chloride 0.13%), 1000 per case, Acme United Corporation, 2280 Tanner Road, Rocky Mou
Hazard: CGMP Deviations
March 11, 2026DrugsFDA
ACME UNITED CORPORATION recalls WP WipesPlus Hand Sanitizing Wipes (Benzalkonium Chloride 0.13%), 5x7, 100 CT, Progressive Products, 211 S. Ridge Street
Hazard: CGMP Deviations
March 11, 2026DrugsFDA
ACME UNITED CORPORATION recalls Med-Nap Cleansing Towelettes (Benzalkonium Chloride 0.13%), 100 Towelettes, Manufactured by: Acme United Corporation, 1
Hazard: CGMP Deviations
March 11, 2026DrugsFDA
ACME UNITED CORPORATION recalls Cleansing Towelette (Benzalkonium Chloride 0.13%), 5"x 7", 1,000 case/Bulk, Med-Nap, Brooksville, FL 34601, Made in USA,
Hazard: CGMP Deviations
March 11, 2026DrugsFDA
ACME UNITED CORPORATION recalls Dynarex Obstetrical Towelettes Cleanser (Benzalkonium Chloride 0.13%), 100 packets, 5" x 7", Manufactured for Dynarex Co
Hazard: CGMP Deviations