
FDA•MODERATE
QuickVue Dipstick Strep A Test
Quidel is recalling QuickVue Dipstick Strep A Test (REF 20108) due to risk of false positive results.

Quidel is recalling QuickVue Dipstick Strep A Test (REF 20108) due to risk of false positive results.

Stryker is recalling the FluidSmart Urology Tube Set (REF LL0006) due to the distribution of nonconforming products.

Hologic recalls Selenia Dimensions mammography systems over loose or broken internal bolts.
2 products
Pure Ground Ingredients recalls Organic Peppermint Leaf Powder over possible Salmonella contamination.

Ascend Laboratories is recalling 25 mg Metoprolol Succinate Extended-Release Tablets due to failed dissolution testing.

Dexcom recalls G7 CGM iOS App (v2.9.0–2.11.2) over glucose alert delays that may cause missed hypo/hyperglycemic events.
4 products
Endo USA recalls Buprenorphine Hydrochloride Injection 0.3mg/mL vials (NDC 42023-179-05) due to particulate matter contamination.

Diowave 250W Laser System recalled; software update needed to correct power output exceeding FDA-cleared 60W limit.

Jolife AB is recalling LUCAS 2, 3, and 3.1 chest compression systems due to missing service documentation.
2 products
Crawford Sausage headcheese may be contaminated with Listeria; produced Jan 20, 2026.
3 products
MG217 Multi-Symptom Treatment Cream recalled due to Staphylococcus aureus contamination.

Oasis Tears PF eye drops (NDC 42126-6400-1) recalled due to lack of assurance of sterility.

Dakota Honey recalls Spreadable Spun Honey varieties over possible metal/plastic contamination.
5 products
GE HealthCare recalls Revolution Ascend CT over AW Server security vulnerability.
7 products
Medline recalls Namic Angiographic Manifolds (SKU 64038200) due to particulate in the fluid path.
14 products
Finesaler recalls Alain Milliat Orange Marmalade 300g jars over possible glass contamination.

DonJoy IceMan Classic Cube recalled due to broken connector interrupting cold therapy.
4 products
On-X is recalling Model ONXMC-25/33 Mitral Heart Valve due to incomplete testing before distribution.

Stoltzfus Family Farm is recalling 8-ounce Sour Cream and Onion cheese curds due to potential Salmonella contamination.

White Cheddar Seasoning recalled over possible Salmonella from milk powder.
2 products
Legacy Bakehouse recalls bagel crisps and pita chips over Salmonella risk from milk powder.
3 products
George J Howe recalls sunflower seed products due to undeclared cashew allergen.
6 products
The Brownie Baker is recalling Cafe Nouria Blueberry Muffin due to undeclared walnuts, which pose a risk to those with nut allergies.

Lundberg Family Farms recalls White Jasmine Rice 32 oz over possible foreign material contamination.

Orthorebirth recalls BioCera Fibers bone void filler (REFs ORB-0320C-KC, ORB-0310C-KC, ORB-0304C-KC, ORB-0302C-KC, ORB-0305D-KC) for out-of-spec.
2 products
Medline is recalling Ancillary Pack-LF and Open Heart Anesthesia ICC-A kits due to potential issues with sterilization and packaging calibration.
58 products
JCB Flavors recalls seasonings over Salmonella risk.
11 products
Hoosier Processing is recalling Albright's All Natural Raw Pet Food Chicken Recipe for Dogs due to potential Salmonella contamination.

Good & Gather Sesame Teriyaki Chicken with Rice recalled due to undeclared sesame allergen.

Givaudan recalls bulk cheese sauce seasoning containing recalled nonfat dry milk powder.

Breckenridge Pharmaceutical is recalling Duloxetine 60mg capsules distributed nationwide due to the presence of an impurity above FDA limits.

Publix Bran Flakes Wheat Cereal recalled over possible plastic contamination.

Acella Pharmaceuticals is recalling Naproxen Oral Suspension, 125 mg/5mL, distributed nationwide due to lead and lithium contamination.

BioFire is recalling the Joint Infection (JI) Panel due to contamination that may cause false positive test results.
Mint Medical is recalling Mint Lesion software versions 3.4.0–3.9.5 due to a risk of data loss or incorrect patient information linking.

One Step 10A in vitro diagnostic test recalled for lack of FDA clearance.
7 products
American Contract Systems is recalling Coronary Angio Packs due to a syringe adaptor defect that may cause disconnection and serious injury.

BioFire is recalling the Spotfire Respiratory/Sore Throat Panel due to the risk of false negative results and control failures.

Medical Action Industries is recalling Pack Cath BHH kits due to a potential syringe adapter disconnection issue.

Katalyst Surgical recalls DEX Ophthalmic Tissue Forceps, model DVF4005-23, due to IFU corrective action.
12 products
My Wife's Slaw (original and Jalapeno Heat) recalled for lack of approved food establishment inspection.
2 products
Market of Choice recalls Vegan Kale Caesar Salad over undeclared sesame allergen.

Shining Sea Fish recalls MA Cohen's Kippered Herring due to botulism hazard.

John B. Sanfilippo recalls nut mixes over Salmonella risk.
6 products
Winfield's CWB Chocolate Bars recalled over undeclared milk allergen.

Cronus Pharma is recalling Amoxicillin and Clavulanate Potassium oral suspension drops for dogs and cats due to product discoloration.
2 products
Woodstock Organic Shelled Edamame recalled over possible metal pieces.

Teva is recalling Octreotide Acetate 30 mg injection kits due to a lack of assurance of sterility.
2 products
California Dairies recalls non-fat dried milk and buttermilk powders over possible Salmonella contamination.
3 products
Rising Pharma is recalling Enalapril Maleate 20 mg tablets (NDC 64980-688-10) due to failed impurities test.
