Latest Product Recalls Today

Recent Product Recall Alerts List

Showing 4,276 - 4,300 of 4,622 matching product recalls.

Product Recall	Source	Type	Risk	Date	Action
Fixone Hybrid Anchor Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.	FDA Z-1166-2026	Medical Device	High	Feb 4, 2026 Recall: Dec 17, 2025	Details
Fixone Biocomposite Anchor Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.	FDA Z-1167-2026	Medical Device	High	Feb 4, 2026 Recall: Dec 17, 2025	Details
BEAR Implant. Model Number: 1000. Incorrect expiration date on label that extends beyond the product's documented/approved shelf life. With an incorrect expiration date, the UDI will also be incorrect.	FDA Z-1220-2026	Medical Device	High	Feb 4, 2026 Recall: Dec 31, 2025	Details
Evolution Upgrade 1.5T. Product Codes (REF): (1) 782148, (2) 782116. MR systems with SW version R11.1 and R12.1. The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS).	FDA Z-1204-2026	Medical Device	High	Feb 4, 2026 Recall: Dec 3, 2025	Details
Medline medical procedure convenience kits labeled as: 1) SMJ LAP CHOLE PACK-LF, Kit SKU DYNJ19974P; 2) DEPAUL ABDOMINAL ENDOSCOPY-LF, Kit SKU DYNJ20027K; 3) LAPAROSCOPY PACK-LF, Kit SKU DYNJ20468J; 4) SMJ LAPAROSCOPY PACK, Kit SKU DYNJ25763N; 5) SMJ LAPAROSCOPY PACK, Kit SKU DYNJ25763O; 6) BWNBORO LAP CHOLE PACK-LF, Kit SKU DYNJ32836B; 7) MINOR SET UP PACK, Kit SKU DYNJ43272K; 8) PK, GEN LAPAROSCOPIC CHOLE, Kit SKU DYNJ43976C; 9) GV LAP CHOLE PACK, Kit SKU DYNJ46939Q; 10) LAP CHOLE PACK, Kit SKU DYNJ49688C; 11) GENERAL ROBOTIC LAP, Kit SKU DYNJ51347N; 12) LAP CHOLE PACK, Kit SKU DYNJ54081F; 1 Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of MASTISOL Liquid Adhesive.	FDA Z-1191-2026	Medical Device	High	Feb 4, 2026 Recall: Dec 12, 2025	Details
Medline medical procedure convenience kits labeled as: 1) BREAST-HERNIA-PORT CDS-LF, Kit SKU CDS984853L; 2) BREAST BIOPSY PACK, Kit SKU DYNJ45641B; 3) DERMATOLOGY PACK, Kit SKU DYNJT3658A. Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of MASTISOL Liquid Adhesive.	FDA Z-1189-2026	Medical Device	High	Feb 4, 2026 Recall: Dec 12, 2025	Details
Brand Name: Broselow Product Name: Broselow Pediatric Emergency Rainbow Tape Model/Catalog Number: 7700RE Software Version: Not Applicable Product Description: The Broselow Tape is a length- and weight-based reference tool specifically designed for pediatric emergency care. Component: No Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine.	FDA Z-1115-2026	Medical Device	High	Feb 4, 2026 Recall: Dec 15, 2025	Details
Interventional Fluoroscopic X-Ray System: LUMINOS Q.namix R; Siemens Material Number (SMN): 11574002; With Software Version VB10D-SP02 Ortho images acquired with preset automatic horizontal flip are not flipped and when acquiring single images, there is the possibility that an image of a previous patient may be processed.	FDA Z-1174-2026	Medical Device	High	Feb 4, 2026 Recall: Dec 29, 2025	Details
Ingenia Ambition S. Product Code (REF): 782108. MR systems with SW version R11.1 and R12.1. The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS).	FDA Z-1209-2026	Medical Device	High	Feb 4, 2026 Recall: Dec 3, 2025	Details
Genesis Push-In Suture Anchor Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.	FDA Z-1171-2026	Medical Device	High	Feb 4, 2026 Recall: Dec 17, 2025	Details
SmartPath to dStream for 3.0T. Product Code (REF): 782145. MR systems with SW version R11.1 and R12.1. The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS).	FDA Z-1215-2026	Medical Device	High	Feb 4, 2026 Recall: Dec 3, 2025	Details
Medline medical procedure convenience kits labeled as: NERVE BLOCK TRAY 2, Kit SKU DYNJRA2713 Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of MASTISOL Liquid Adhesive.	FDA Z-1186-2026	Medical Device	High	Feb 4, 2026 Recall: Dec 12, 2025	Details
AlternatiV+ Screw-In Anchor Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.	FDA Z-1173-2026	Medical Device	High	Feb 4, 2026 Recall: Dec 17, 2025	Details
Medline medical procedure convenience kits labeled as: 1) WATKINS SPINE PACK-LF, Kit SKU DYNJ0275635M; 2) SM-SPINE PACK-LF, Kit SKU DYNJ0395037X; 3) TOTAL HIP PACK, Kit SKU DYNJ04809N; 4) MAIN/LAMINECTOMY PACK-LF, Kit SKU DYNJ0565499AN; 5) SCC/SPOC HAND & FOOT PACK, Kit SKU DYNJ27164Q; 6) ORTHO SPINE, Kit SKU DYNJ40221G; 7) URO GYN PACK, Kit SKU DYNJ45311J; 8) LAMINECTOMY PACK, Kit SKU DYNJ46330C; 9) DJ ORTHO SPINE, Kit SKU DYNJ48980M; 10) CERVICAL PACK, Kit SKU DYNJ52995F; 11) NORTH BACK FUSION PACK-LF, Kit SKU DYNJ56483L; 12) KNEE ARTHROSCOPY CHRISTUS, Kit SKU DYNJ61200B; 13) KNEE ARTHROSCOP Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of MASTISOL Liquid Adhesive.	FDA Z-1200-2026	Medical Device	High	Feb 4, 2026 Recall: Dec 12, 2025	Details
LSL Healthcare, Central Line Dressing Kit, Model/Catalog Number: 2519CP, medical procedure convenience kit BD ChloraPrep Triple Swabsticks, a component within the kits, exhibit an open seal on the packaging of the applicators.	FDA Z-1219-2026	Medical Device	High	Feb 4, 2026 Recall: Dec 22, 2025	Details
Roasted Pumpkin & White Cheddar Tamales Ingredients: Organic Corn Flour Masa, Pumpkin, Green Chile, Sharp Cheddar Cheese (Pasteurized Milk, Cheese Cultures, Salt and Enzymes), Butter, Salt, Spices, Baking Powder (Sodium Acid Pyrophosphate, Sodium Bicarbonate, Corn Starch and Monocalcium Phosphate). Contains Milk Microwave: In husk approx. 90 seconds per tamale. Steam: In husk approx. 15 minutes. Primavera 17070 Sonoma Hwy. Sonoma, CA 95476 (707) 939-9350 Perishable Keep Refrigerated Net Wt. 24oz. UPC: 748732000263 Potential contamination with biological hazards (Listeria monocytogenes).	FDA H-0425-2026	Food	High	Feb 4, 2026 Recall: Dec 12, 2025	Details
Goldenroot Lemon Ginger Hibiscus Ginger Beer. 12 oz. (355 ml) UPC 8 50052-32821 4. Keep Cold. Manufactured By Goldenroot, 3841 Market St #113, Denton, TX 76209. Ginger Beer products might contain ginger juice that did not undergo the required pasteurization process.	FDA H-0437-2026	Food	High	Feb 4, 2026 Recall: Dec 8, 2025	Details
Hannaford hamburger dill pickle chips 16 FL OZ (1 PT) 473mL glass jar. UPC 0 41268 14889 9 DISTRIBUTED BY: HANNAFORD BROS. CO. SCARBOROUGH, ME 04074 Glass in Pickles. The firm received complaints of glass found in the product.	FDA H-0422-2026	Food	High	Feb 4, 2026 Recall: Jan 7, 2026	Details
Qunol, Extra Strength Turmeric Capsule, 1000mg ,HDPE bottle with cap, BIO7771 120 count bottle, BIO7772 120 count bottle ,BIO8281 60 count bottle . Mold contamination detected for raw material lots that were produced in July and used in finished goods.	FDA H-0418-2026	Food	High	Feb 4, 2026 Recall: Dec 16, 2025	Details
Mushroom, Spinach & Salsa Tamales No Dairy Ingredients: Organic Corn Flour Masa, Mushrooms, Spinach, Tomatoes, Onions, Jalapenos, Non-hydrogenated Vegetable Shortning, Salt, Spices, Baking Powder. Microwave: In husk approx. 90 seconds per tamale. Steam: In husk approx. 15 minutes. Primavera 17070 Sonoma Hwy. Sonoma, CA 95476 (707) 939-9350 Perishable Keep Refrigerated Net Wt. 24oz. UPC: 748732000317 Potential contamination with biological hazards (Listeria monocytogenes).	FDA H-0426-2026	Food	High	Feb 4, 2026 Recall: Dec 12, 2025	Details
BBQ Chipotle Bean & White Cheddar Tamales Ingredients: Organic Corn Flour Masa, Beans, Jack Cheese (Pasteurized Milk, Cheese Cultures, Salt and Enzymes), Salsa (Tomatoes, Onions, Chiles, Garlic & Cilantro), Butter, Non-GMO Corn, Salt, Spices, Baking Powder (Sodium Acid Pyrophosphate, Sodium Bicarbonate, Corn Starch and Monocalcium Phosphate). Microwave: In husk approx. 90 seconds per tamale. Steam: In husk approx. 15 minutes. Primavera 17070 Sonoma Hwy. Sonoma, CA 95476 (707) 939-9350 Perishable Keep Refrigerated Net Wt. 24oz. UPC: 748732000256 Potential contamination with biological hazards (Listeria monocytogenes).	FDA H-0427-2026	Food	High	Feb 4, 2026 Recall: Dec 12, 2025	Details
Preserved Mustard in Soybean Oil; original packaging is predominantly green with gold accents and black Chinese lettering. UPC: 6 927393 804265 Undeclared allergen ingredient (wheat).	FDA H-0420-2026	Food	High	Feb 4, 2026 Recall: Nov 19, 2025	Details
Goldenroot Lemon Ginger Elderberry Ginger Beer. 12 oz. (355 ml) UPC 8 50052-32818 4. Keep Cold. Manufactured By Goldenroot, 3841 Market St #113, Denton, TX 76209. Ginger Beer products might contain ginger juice that did not undergo the required pasteurization process.	FDA H-0435-2026	Food	High	Feb 4, 2026 Recall: Dec 8, 2025	Details
HIGHER HARVEST by H-E-B brand; Dairy Free Coconut Based YOGURT; STRAWBERRY; YOGURT ALTERNATIVE; NET WT 5.3 OZ; INGREDIENTS: COCONUT MILK (WATER, COCONUT CREAM, MODIFIED TAPIOCA STARCH), STRAWBERRIES, CANE SUGAR, WATER, STARCH, NATURAL FLAVOR, FRUITS AND VEGETABLE JUICE (FOR COLOR) LOCUST BEAN GUM, LEMON JUICE CONCENTRATE, LIVE AND ACTIVE CULTURES, VITAMIN B12; CONTAINS: COCONUT Contains undeclared Almonds	FDA H-0421-2026	Food	High	Feb 4, 2026 Recall: Dec 17, 2025	Details
a.) Live it Up brand Super Greens; Natural Wild Berry Flavor; Chlorella, Spirulina, Wheatgrass, Kale, Broccoli, Spinach, Barley grass, Moringa, Parsley; Whole food dietary supplement powder; 30 day supply; NET WT. 9.49oz (269.16g); Manufactured for Superfoods, Inc.; UPC: 860013190811 b.) Live it Up brand Super Greens; Natural Wild Berry Flavor; Chlorella, Spirulina, Wheatgrass, Kale, Broccoli, Spinach, Barley grass, Moringa, Parsley; Whole food dietary supplement powder; 30-0.32oz (9g) STICKS - NET WT. 9.52oz (270g); Manufactured for Superfoods, Inc.; UPC: 850077468070 Products may be contaminated with Salmonella Typhimurium	FDA H-0434-2026	Food	High	Feb 4, 2026 Recall: Jan 15, 2026	Details

Showing 4,276 - 4,300 of 4,622 product recalls

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