State
72,940 recalls have nationwide distribution and so reach Minnesota. 7,804 additional recalls listed Minnesota specifically in their distribution scope.
Of the 7,804 recalls naming Minnesota we have scored against our rubric, 1,125 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,892 (24%) are Severe.
Which agencies issued them
These figures cover only the 7,804 recalls whose distribution notice names Minnesota specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Smith & Nephew is recalling 168 BIOSURE HA Screws, 6mm x 20mm, due to a labeling error on the affected lot.
Sun Pharma/Taro is recalling 17,664 units of Ciclopirox Shampoo 1% after out of specification impurity and degradation results at the 18-month timepoint.
Novocol Pharmaceutical of Canada is recalling 5,520 cartons of Mepivacaine HCl 3% injection over a defective container with cracked or broken cartridges.
DSAART is recalling 29 AART Chin Implants because the products deviated from established specifications and were distributed without the required FDA premarket approvals or clearances.
Somerset Therapeutics is recalling 71,310 vials of Cisatracurium Besylate Injection, 20 mg/10 mL, after out of specification assay results during long term stability testing.
Somerset Therapeutics is recalling 28,660 vials of Cisatracurium Besylate Injection, 200mg/20mL, after out of specification assay results during long term stability testing.
Novocol Pharmaceutical of Canada is recalling 5,825 units of 3% Polocaine Dental mepivacaine injection over a defective container with cracked or broken cartridges.
DSAART is recalling 35 AART Calf Implants because the products deviated from established specifications and were distributed without the required FDA premarket approvals or clearances.
DSAART is recalling 369 AART Silicone Carving Implants because the products deviated from established specifications and were distributed without the required FDA premarket approvals or clearances.
DSAART is recalling 2 AART Malar Implants because the products deviated from established specifications and were distributed without the required FDA premarket approvals or clearances.
Myofunctional Research Company USA is recalling 436 Myosa for Kids devices because the firm mistakenly distributed the product within the US without FDA premarket clearance or approval.
Copan Italia is recalling 122,850 units of 1ml DTT liquid reagent because treatment reagent functionality in respiratory specimens fluidification cannot be guaranteed.
Novocol Pharmaceutical of Canada is recalling Mepivacaine HCl 3% injection distributed by Benco Dental over a defective container with cracked or broken cartridges.
Somerset Therapeutics is recalling 52,340 vials of Cisatracurium Besylate Injection, 10 mg/5 mL, after out of specification assay results during long term stability testing.
DSAART is recalling 118 AART Gluteal Implants because the products deviated from established specifications and were distributed without the required FDA premarket approvals or clearances.
Novocol Pharmaceutical of Canada is recalling 1,636 cartons of OraVerse (Phentolamine Mesylate) Injection over a defective container with cracked or broken cartridges.
Novocol Pharmaceutical of Canada is recalling 18,789 cartons of 2% Xylocaine Dental with Epinephrine over a defective container with cracked or broken cartridges.
Novocol Pharmaceutical of Canada is recalling 40 cartons of Cook-Waite Carbocaine 3% mepivacaine injection over a defective container with cracked or broken cartridges.
Novocol Pharmaceutical of Canada is recalling 12,033 cartons of Lidocaine HCl 2% with Epinephrine 1:100,000 injection over a defective container with cracked or broken cartridges.
DSAART is recalling 41 AART Pectoral Implants because the products deviated from established specifications and were distributed without the required FDA premarket approvals or clearances.
Datascope is recalling 47 Cardiosave Rescue units to issue an instructions for use addendum updating the Vibration and Shock Table to reference the correct standards.
Datascope is recalling 11,470 Cardiosave Hybrid units to issue an instructions for use addendum updating the Vibration and Shock Table to reference the correct standards.
Altec is recalling 2022-2023 AA55, AM55, AN46, and AN55 vehicles because a missing check valve may reduce boom insulation, increasing the risk of electric shock.
BMW is recalling one 2025 i4 eDrive40 vehicle because the connection between the positive battery cable and the rear power distributor may become loose.
KTM is recalling certain 2025 390 Adventure R, 390 Adventure X, 390 SMC R and 390 Enduro R motorcycles because engine vibrations may break the side stand spring, letting the stand fall to the ground.