Health & Personal Care
HIGH
FDA DEVICE
Philips Medical Systems Nederland Blames BIOS Battery Design Flaw in Allura Centron 722400 Recall (Z
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
The BIOS
pet related Recalls
225 recalls tagged with “pet related”.
Health & Personal Care
HIGH
FDA DRUG
Major Pharmaceuticals Sulfamethoxazole and Trimethoprim 800 mg/160 mg 100-Tablets Recall 2025
Presence of a Foreign Substance: A specific lot of auxiliary polyester coil, used in product packaging by manufacturer (Amneal Pharmaceuticals LLC) was detected with presence of a micro-organism. No micro-organism was detected on any tablets.
Sulfamethoxazole and Trimethoprim
Presence of
Health & Personal Care
HIGH
FDA DEVICE
Northeast Scientific NES Reprocessed 2.0mm RX Turbo Elite Laser Atherectomy Catheter Recall 2026
Potential for breaches in the sterile barrier packaging, compromising sterility assurance.
Northeast Scientific
Potential for
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
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
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
Northeast Scientific Recalled 1,019 Reprocessed Turbo Elite Atherectomy Catheters Over Sterility Bre
Potential for breaches in the sterile barrier packaging, compromising sterility assurance.
Northeast Scientific
Potential for
MEDIUM
CPSC
DT Swiss Recalls Carbon Wheels Over Crash Hazard Affecting 2740000 ID Codes and Higher (2025)
DT Swiss
A defect
Health & Personal Care
HIGH
FDA DEVICE
Boston Scientific Extractor Pro RX Balloon Catheter Recalled Over Labeling Error (2025)
The product in incorrectly labeled. The label indicates that the skive hole should be above the balloon, while it is actually positioned below, and vice versa.
Boston Scientific
The product
Health & Personal Care
HIGH
FDA DEVICE
Siemens MAGNETOM Lumina MRI System Recall Covers 71 Units Worldwide for Ice Blockage Risk
Siemens Medical Solutions USA recalled 71 MAGNETOM Lumina MRI systems worldwide, including US and 50+ countries, due to ice blockage in the magnet venting system that could cause a helium leak during a quench.
Siemens Medical Solutions USA
There is
Health & Personal Care
HIGH
FDA DEVICE
Siemens Biograph mMR PET-MRI Recall 2025 for Ice Blockage Risk in Venting System (23 Units)
Siemens
There is
Health & Personal Care
HIGH
FDA DEVICE
Siemens MAGNETOM Connectom.X MRI Recalled Globally Over Ice Blockage in Vent System
Siemens Medical Solutions USA
There is
Health & Personal Care
HIGH
FDA DEVICE
Siemens MRI Recall: 18 MAGNETOM Skyra Fit BioMatrix Systems Recalled Over Helium Vent Blockage Risk
Siemens Medical Solutions USA
There is
Health & Personal Care
HIGH
FDA DEVICE
Siemens Medical Solutions USA BIOGRAPH One MRI System Recalled for Helium Leak Risk (1 Unit, 2025)
Siemens Medical Solutions USA
There is
Health & Personal Care
HIGH
FDA DEVICE
Siemens MAGNETOM Verio Dot Upgrade MRI Recalled Over Ice Blockage Risk (46 Units) 2025
Siemens Medical Solutions USA
There is
Health & Personal Care
HIGH
FDA DEVICE
Siemens MAGNETOM Skyra MRI System Recall Covers 182 Units Over Ice Blockage Risk
Siemens Medical Solutions USA
There is
Food & Beverages
HIGH
FDA FOOD
Middlefield Original Cheese Cooperative Smoked Cheddar Recalled for Listeria Risk in 2025
Potential contamination with Listeria monocytogenes
Middlefield Original Cheese Cooperative
Potential contamination
Health & Personal Care
HIGH
FDA DRUG
Unichem Pharmaceuticals USA Cyclobenzaprine Recall for Label Mix-Up Affects 230 Bottles (2025)
Labeling: Label Mix Up; Bottles of Meloxicam USP, 7.5mg, 90-count tablets (yellow in color), were labeled as Cyclobenzaprine Hydrochloride Tablets USP, 10 mg 90-count tablets (blue in color).
CYCLOBENZAPRINE HYDROCHLORIDE
Labeling: Label
Food & Beverages
HIGH
FDA FOOD
Middlefield Original Cheese Cooperative Recalls 5 lb Shredded Mozzarella Over Listeria Risk (2025)
Potential contamination with Listeria monocytogenes
Middlefield Original Cheese Cooperative
Potential contamination
Food & Beverages
HIGH
FDA FOOD
Middlefield Original Cheese Cooperative Recalls 7,455 lbs Shredded Mozzarella/Provolone (5-lb Bags)
Potential contamination with Listeria monocytogenes
Middlefield Original Cheese Cooperative
Potential contamination
Tag Statistics
Total Recalls
225