State
73,576 recalls have nationwide distribution and so reach Indiana. 9,592 additional recalls listed Indiana specifically in their distribution scope.
Of the 9,592 recalls naming Indiana we have scored against our rubric, 1,913 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,529 (26%) are Severe.
Which agencies issued them
These figures cover only the 9,592 recalls whose distribution notice names Indiana specifically. The 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
TJX is recalling about 92,000 outdoor wooden folding chairs because they can break or collapse, posing fall and injury hazards.
Smiths Medical ASD Inc. is recalling 250 units of ACE MDI Spacers with Small Masks because shipping box labels may be incorrect.
Cardiac Assist, Inc. is recalling 13 Protek Solo Venous Dilator Sets due to incorrect packaging discovered in finished goods.
Smith & Nephew is recalling CANNU-Flex SILK Interference Screws because some boxes were mislabeled, containing 6mm x 20mm screws instead of the labeled 6mm x 30mm size.
Siemens Medical Solutions is recalling 772 Artis zee ceiling-interventional Fluoroscopic X-Ray Systems due to increased cabling abrasion that may limit functionality and disrupt clinical treatment.
Smiths Medical ASD Inc. is recalling 682 Palm Cups because shipping box labels may be incorrect. The devices are intended to mobilize bronchial secretions.
Change Healthcare is recalling Enterprise Viewer software versions 2.0 and 2.1 due to a defect that may prevent anchor studies from displaying.
DJ Orthopedics is recalling Donjoy Ultrasling Pro arm slings because a rivet at the chafe tab may fail. The recall covers units distributed in the US and several international countries.
Nextremity Solutions is recalling 123 units of InCore Lapidus Disposable Kits because a drill bushing defect may prevent surgeons from completing the intended procedure.
Datascope Corp. is recalling Cardiosave Rescue IABP units due to cybersecurity vulnerabilities in a TCP/IP software library that may cause loss of communication to hospital systems.
Nextremity Solutions is recalling 111 units of the InCore Lapidus Disposable Kit 28mm Left because a drill bushing defect may prevent surgeons from completing the intended procedure.
Ortho-Clinical Diagnostics is recalling VITROS Black Reference Slides incorrectly labeled as White Reference Slides, which may cause analyzer delays.
Cytocell Ltd. is recalling 89 Chromosome X Alpha-Satellite probes because users may observe additional signals at 9q34, contradicting the insert.
Siemens is recalling 133 ARTIS X-ray systems due to a potential software issue that may require terminating planned procedures.
Coltene Whaledent Inc is recalling TMS LINK PLUS Self-Threading Dental Pins because incorrect pins were packaged and distributed. The recall affects 65 packs of 20 pins.
Teligent Pharma is recalling Betamethasone Dipropionate Ointment 0.05% due to failed impurity specifications. The product is distributed nationwide in 15-gram tubes.
Boston Scientific is recalling three EXALT Controllers because they may have been programmed with suboptimal brightness settings, resulting in darker than desired images.
Medela is recalling AXS Universal Aspiration Tubing because the label displays an incorrect expiration date of 2023-07-24 instead of 2021-07-24.
Genentech is recalling 2,627 bottles of Evrysdi (risdiplam) for oral solution because some have incorrect press-in-bottle-adapters that do not fit co-packed syringes.
Teligent Pharma is recalling 79,416 tubes of Betamethasone Dipropionate Ointment USP, 0.05% (Augmented) because the product failed impurity specifications.
Teligent Pharma is recalling Betamethasone Dipropionate Ointment 0.05% because it failed impurity specifications for a known degradation product.
Bellisio Foods is recalling approximately 3,927 pounds of Michelina's Spaghetti with Meat Sauce due to misbranding and an undeclared soy allergen.
Chrysler is recalling the 2020 Alfa Romeo Stelvio due to a defect in the anti-lock braking system. Hard braking can cause the ABS hydraulic control unit rotor shaft to separate, reducing braking performance and increasing crash risk.
Ducati is recalling specific 2016-2020 models because air may enter the rear brake system, reducing braking effectiveness and increasing crash risk.
Blue Bird is recalling 2018-2022 All American buses because a fuel rail leak could cause a fire. Owners should contact dealers for free repairs.