Food & Beverages
HIGH
FDA FOOD
Tas Tematic Foods Frozen Shrimp IQF 2-lb Bags Recalled for Nitrofuran Contamination (2025)
Product which was on FDA hold for high levels of Nitrofuran was inadvertently distributed.
Tas Tematic Foods
Product which
These recalls involve products that pose serious risks of injury or death. Check if you own any of these products and take immediate action if needed.
Immediate attention
High Risk Recalls
3,585 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
- High-risk recalls
- 3,585
- Action level
- Stop use
What to do if you own a recalled product
- Stop using the product immediately
- Keep the product away from children
- Follow the remedy instructions provided
- Contact the manufacturer for a refund or replacement
Health & Personal Care
HIGH
FDA DEVICE
Northeast Scientific Laser Atherectomy Catheter Recalled for Sterile Barrier Breach Risk (2025)
Potential for breaches in the sterile barrier packaging, compromising sterility assurance.
Northeast Scientific
Potential for
Health & Personal Care
HIGH
FDA DEVICE
Baxter Healthcare CLEARLINK CONTINU-FLO IV Set Recalled for Leaks in 2025 (958,351 Units)
Baxter Healthcare
IV sets
Health & Personal Care
HIGH
FDA DEVICE
Baxter Healthcare's CLEARLINK CONTINU-FLO IV Set Recall for Leakage Risk (2025)
Baxter Healthcare Corp. recalled 12,720 CLEARLINK SYSTEM CONTINU-FLO IV sets distributed nationwide to healthcare facilities. The devices may leak during use. Hospitals and clinicians should stop using immediately and follow Baxter's recall instructions.
Baxter Healthcare
IV sets
Health & Personal Care
HIGH
FDA DEVICE
Baxter Healthcare CLEARLINK CONTIN-FLO IV Solution Sets Recalled for Leaks (2025)
Baxter Healthcare
IV sets
Health & Personal Care
HIGH
FDA DEVICE
Baxter Healthcare Recalls 8,368 CLEARLINK CONTINU-FLO IV Sets for Leakage Risk (2025)
Baxter Healthcare
IV sets
Health & Personal Care
HIGH
FDA DEVICE
Baxter Healthcare CLEARLINK CONTIN-FLO IV Infusion Sets Recalled for Leaks (106,176 Units)
Baxter Healthcare
IV sets
Health & Personal Care
HIGH
FDA DEVICE
Baxter Healthcare Recalls 15,552 CLEARLINK IV Extension Sets for Leakage Risk (2025)
Baxter Healthcare recalled 15,552 CLEARLINK SYSTEM EXTENSION SETS nationwide in the United States. The IV extension sets may leak. Healthcare providers and patients should stop using the device immediately and follow Baxter recall instructions.
Baxter Healthcare
IV sets
Health & Personal Care
HIGH
FDA DEVICE
Northeast Scientific NES Reprocessed 0.9mm Turbo Elite Laser Atherectomy Catheter Recall 2025
Potential for breaches in the sterile barrier packaging, compromising sterility assurance.
Northeast Scientific
Potential for
Health & Personal Care
HIGH
FDA DEVICE
Northeast Scientific Recalled 561 Units of NES Reprocessed 0.9mm OTW Turbo Elite Laser Atherectomy C
Potential for breaches in the sterile barrier packaging, compromising sterility assurance.
Northeast Scientific
Potential for
Health & Personal Care
HIGH
FDA DEVICE
ImaCor ClariTEE Miniaturized TEE Probe CLT-010 Recalled Over Reversed Articulation Risk (2025)
Production assembly error resulting in the potential for reversed articulation, where moving the lever forward caused the probe tip to anteflex rather than retroflex, and vice versa.
ImaCor
Production assembly
Food & Beverages
HIGH
FDA FOOD
Rolling Pin Baking Company Recalls 127,680 Dubai Style Chocolate Pouches for Undeclared Wheat (2025)
Product does not declare wheat in the allergen statement.
Rolling Pin Baking Company
Product does
Health & Personal Care
HIGH
FDA DEVICE
Baxter recalls 2,304 CLEARLINK IV Extension Sets for leak risk in 2025
Baxter Healthcare
IV sets
HIGH
CPSC
Party Favors Lite-Up Torches and Laser Pointers Recalled for Battery Ingestion Risk
Party Favors recalled four models of lite-up torches and laser pointers due to risk of serious injury or death from swallowed button cell batteries. Imported by MTC Trading. Consumers should stop using the products and seek a full refund.
Party Favors Lite-Up Torches and Laser Pointers
The recalled
Health & Personal Care
HIGH
FDA DRUG
Granules Pharmaceuticals Amphetamine Salts Recall Over Impurities Degradation Specifications (2025)
Dextroamphetamine Saccharate
Failed Impurities/Degradation
HIGH
Health & Personal Care
HIGH
FDA DRUG
Granules Pharmaceuticals Recalls 3,384 Bottles of Dextroamphetamine ER Capsules for Impurity Issues
Granules Pharmaceuticals
Failed Impurities/Degradation
Health & Personal Care
HIGH
FDA DRUG
Granules Pharmaceuticals Dextroamphetamine Mixed Salts ER Capsules Recall 11,909 Bottles (2025)
Granules Pharmaceuticals
Failed Impurities/Degradation
Health & Personal Care
HIGH
FDA DRUG
Granules Pharmaceuticals Recall: 11,928 Bottles of Dextroamphetamine Mixed Salts Suspended for Impur
Granules Pharmaceuticals
Failed Impurities/Degradation
Health & Personal Care
HIGH
FDA DRUG
Granules Pharmaceuticals Amphetamine Capsules Recalled for Impurities Degradation Standards (2025)
Granules Pharmaceuticals
Failed Impurities/Degradation