Recalls distributed in Indiana
These notices name Indiana in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.
4,253 stored notices name Indiana, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Indiana too — those are in the archive.
Reported Jul 30, 2025
Covidien Nellcor Bedside SpO2 Patient Monitoring System: REF: PM100N, 10005941, DLPM100N, DL10005941, DSPM100N,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien
FDA (openFDA device enforcement)
Reported Jul 30, 2025
Brand Name: EMPOWR Dual Mobility" Product Name: EMPOWR Acetabular, Dual Mobility, Poly Bearing, ID28, OD40…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Encore Medical, LP
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 30, 2025
ACUVUE¿ OASYS MAX 1-Day MULTIFOCAL
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Johnson & Johnson Vision Care, Inc.
FDA (openFDA device enforcement)
Reported Jul 30, 2025
Artisan Style 1/2 Loaf, Net wt. 12 oz (340g) 024126018152 1/2 Loaf of white bread with white flour topping and two…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lewis Bakeries
FDA (openFDA food enforcement)
Reported Jul 30, 2025
Sushi Wasabi; 5 grams (Ready to eat) Ingredients: Horseradish, Corn Oil, Salt, Water, Citric Acid, Tumeric, FD&C Blue#1…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ming Hong International Inc.
FDA (openFDA food enforcement)
Reported Jul 30, 2025
Ritz Peanut Butter Cracker Sandwiches, Net Wt.27.6 oz, 20 count (20x1.38 oz) 6- pack of cracker sandwiches inside…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mondelez Global LLC
3 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 30, 2025
Natus Brain Monitor Breakout Box, Part Number 021911; full-montage standard electroencephalograph
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natus Neurology dba Excel Tech., Ltd. (XLTEK)
FDA (openFDA device enforcement)
Reported Jul 30, 2025
FSIS Issues Public Health Alert for Frozen Pork and Beef Tortellini Product Due to Misbranding and Undeclared Allergens
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.P.E. & F Inc. dba DiMare's Specialty Foods
USDA FSIS
Reported Jul 30, 2025
Azurion 7 M20. Fluoroscopic X-Ray System.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems Nederland B.v.
FDA (openFDA device enforcement)
Reported Jul 30, 2025
Stryker, StrykeFlow , REF: 0250070500, 2, Disposable Suction/Irrigator without Disposable Tip
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 30, 2025
Turkeyfoot Creek Creamery Avalanche Artisan Ice Cream, One Pint (473 ml), packaged individually in a paper carton with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Turkeyfoot Creek Creamery LLC
7 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 23, 2025
Brand Name: EMPOWR 3D KNEE TIBIAL INSERT - E-PLUS Product Name: EMPOWR 3D KNEETM INS, 11L 10MM, VE Model/Catalog…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Encore Medical, LP
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 23, 2025
SwabCap Disinfecting Cap for Needlefree Connectors: SwabSleeve, REF: SCXT3-5-2000; SwabCap, 200-ct. Box, REF: SCXT3-2000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
FDA (openFDA device enforcement)
Reported Jul 23, 2025
i-view video laryngoscope. Model Number: 8008000. The i-view video laryngoscope is indicated to facilitate laryngoscopy.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Intersurgical Inc.
FDA (openFDA device enforcement)
Reported Jul 23, 2025
J. Higgs Potato Chip Mix, 18 1oz singles, net weight 180z., UPC 0-51933-37327-3
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Saratoga Potato Chips LLC
FDA (openFDA food enforcement)
Reported Jul 23, 2025
Wei-Chuan branded Black Fungus Slice. Net weight: 2.5 oz UPC#: 072869231321
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wei-Chuan USA Inc.
FDA (openFDA food enforcement)
Reported Jul 23, 2025
Dubai emek SPREAD PISTACHIO CACAO CREAM WITH KADAYIF NET WT. 9.7oz UPC 8 69652 10130 1 Manufacturer: Emek Dogal Saglik…
High riskUsing this product could cause serious injury, illness or death — stop using it now.World Market Management Services, LLC
FDA (openFDA food enforcement)
Reported Jul 16, 2025
Brand Name: Alcon Laboratories, Inc. Product Name: Constellation Vision System Vitrectomy Procedure Pak Model/Catalog…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alcon Research LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 16, 2025
Brand Name: Canturio¿ Smart Extension Product Name: CSE Implant Model/Catalog Number: 43-5570-030-14 Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Canary Medical, Inc.
FDA (openFDA device enforcement)
Reported Jul 16, 2025
Brand Name: Optisite Arterial Cannula Product Name: Optisite Arterial Cannula Model/Catalog Number: OPTI16 Software…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Edwards Lifesciences, LLC
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 16, 2025
O-arm O2 Imaging System. Mobile X-Ray System.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.-Boxborough
FDA (openFDA device enforcement)
Reported Jul 16, 2025
TrueDent Clear, TDM 100, Model No. OBJ-09164 Light-curable methacrylate-based resin that enables fabrication of dental…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Stratasys Ltd.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 9, 2025
--- Shell Eggs; Brown; Various sizes - medium, large, and jumbo; Various pack sizes - 5, 12, 18, and Loose ---- Clover…
High riskUsing this product could cause serious injury, illness or death — stop using it now.August Egg Company
FDA (openFDA food enforcement)
Reported Jul 9, 2025
REF: 335775 , BD FACS, 7-Color Setup Beads, 25 setups per kit, Rx Only, IVD. Used in flow cytometry for fluorescence…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton, Dickinson and Company, BD Bio Sciences
1 more product in this recall
FDA (openFDA device enforcement)
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RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.