State
73,381 recalls have nationwide distribution and so reach Indiana. 9,587 additional recalls listed Indiana specifically in their distribution scope.
Of the 9,587 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 2,528 (26%) are Severe.
Which agencies issued them
These figures cover only the 9,587 recalls whose distribution notice names Indiana specifically. The 73,381 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Family Dollar Stores is recalling Lidocaine Arthritis and Sport wintergreen liniment (16 fl oz, SKU 902929) distributed nationwide April 30–June 10, 2022, due to improper storage temperature conditions.
Fleet Glycerin Suppositories distributed nationwide from April 30 to June 10, 2022, are being recalled because the product was held outside appropriate storage temperature conditions.
Family Dollar Stores is recalling Alka Seltzer Extra Strength 24 CT due to products stored outside proper temperature conditions, which may affect product quality.
Four topical analgesic products distributed to Family Dollar stores were recalled due to CGMP violations involving improper storage temperature conditions. No illnesses or injuries have been reported.
Good Sense and Prilosec OTC omeprazole tablets distributed by Family Dollar Stores have been recalled due to improper storage temperature conditions. No illnesses have been reported.
Mckesson Medical-Surgical Inc. is recalling Fisherbrand laboratory swabs due to facility temperature excursions from June through August 2021 that may have impacted product effectiveness. All affected lots distributed between June 1 and September 30, 2021 are included.
Family Dollar Stores is recalling Preferred Urinary Pain Relief Max Strength due to CGMP violations involving improper storage temperature. Product was distributed nationwide April 30 through June 10, 2022.
RIC Stool Softener Softgels (SKUs 917000 and 902493) distributed to Family Dollar Stores nationwide from April 30, 2022 through June 10, 2022 are recalled due to improper storage temperature conditions.
Family Dollar Stores is recalling Voltaren Arthritis Pain Gel 20G distributed April–June 2022 due to storage temperature deviations that may affect product effectiveness.
BD Vacutainer blood collection tubes are recalled due to potential temperature damage during storage from June to August 2021. Affected tubes received between June 1 and September 30, 2021 may have reduced effectiveness.
Family Dollar Stores is recalling NPX Enema 4.5 FL OZ 2-packs due to improper storage conditions that violate manufacturing standards. The product was held outside appropriate temperature conditions at select Family Dollar stores between April 30 and June 10, 2022.
Mckesson is recalling a Total-Fix stool collection parasitology kit due to temperature exposure that may have reduced its effectiveness. All lots received between June 1 and September 30, 2021 are affected.
Family Dollar Stores recalled two antifungal products due to storage temperature deviations. The products may have been compromised in effectiveness due to failure to maintain proper storage conditions.
Connoisseur’s Kitchen is recalling approximately 880 pounds of imported frozen ready-to-eat chicken entrees due to possible Listeria monocytogenes contamination. No illnesses have been reported.
Oshkosh is recalling certain Shepphard steering gears for S-Series 2.0 vehicles because incorrect assembly may cause the gear to fracture, potentially leading to a loss of steering control.
REV is recalling 2018-2023 motorhome models from Fleetwood and Holiday Rambler because hydraulic lines may be improperly routed or protected, risking fluid leaks that could cause fires. Dealers will repair free of charge.
Porsche is recalling 2001-2020 models because missing caps on headlight adjustment screws can cause improper alignment, increasing crash risk.
Wayfarer is recalling 2017-2020 Tiffin Wayfarer motorhomes because wheel lug nuts may not have been properly tightened during a previous repair, posing a crash risk.
DRV is recalling 2021-2022 Mobile Suites fifth wheels because tail, stop, and turn lights may be placed too high, reducing visibility and increasing crash risk.
Volkswagen Group of America is recalling 2022 Audi A3, S3, and RS3 vehicles because the front passenger air bag may be folded incorrectly, increasing injury risk in a crash.
Daimler Trucks North America is recalling certain 2020-2023 Western Star 47X and 49X commercial trucks because hood bezel covers may detach, creating a road hazard and increasing crash risk. Approximately 3,498 vehicles are affected.
Cruise LLC is recalling Automated Driving System units with specific software versions that may incorrectly predict vehicle paths during unprotected left turns, increasing crash risk.
Roadtrek is recalling certain 2022 Zion, Zion SRT, Chase, and Zion Slumber motorhomes because front seat mounting bolts may be improperly tightened, potentially failing to restrain occupants during a crash.
Kia is recalling certain 2023 Sportage vehicles because the alternator battery positive terminal nut may loosen, risking engine stall or fire. Dealers will inspect and tighten the terminal nut free of charge.
Ford is recalling 2022 Mustang Mach-E vehicles because the right-rear axle half shafts may break under load, potentially causing loss of drive power or a rollaway.