All recall categories

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.

Food

Reported Nov 2, 2022

Qassim Mix for Coffee, Net Weight 125g, packaged in a plastic container (UPC 6-281103 300011). Each case contains…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Tomoorona LLC

FDA (openFDA food enforcement)

Medical devices

Reported Nov 2, 2022

AutoPulse Li-ion Battery used on the AutoPulse Resuscitation System Model 100. used as an adjunct to manual CPR

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

ZOLL Circulation, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 26, 2022

Product/Part: MitraClip XTR Clip Delivery System US/CDS0601-XTR, MitraClip G4 Clip Delivery System NT US/CDS0701-NT,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Abbott Vascular

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 26, 2022

Mrs. Freshley's Apple Fruit Pie NET WT 4.5 OZ (128g) UPC 0 72250 00817 4 DISTRIBUTED BY FLOWERS FOODS SPECIALTY GROUP,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Flowers Foods (Corporate Offices)

5 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Oct 26, 2022

Lyons Ready Care Thickened Apple Nectar packaged in combi-bloc multi wall paper cartons 46 fl oz cartons - 6 cartons to…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Lyons Magnus LLC

11 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Oct 26, 2022

"***Nestle***STUFFED***CHOCOLATE CHIP COOKIE DOUGH***4 JUMBO COOKIES***NET WT 8 OZ***"

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Nestle-USA, Inc. (Corporate Office)

FDA (openFDA food enforcement)

Food

Reported Oct 26, 2022

Seeking Health brand Optimal Multivitamin Chewable Dietary Supplement tablets, 60 chewable tablets per package. Product…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Seeking Health LLC

FDA (openFDA food enforcement)

Food

Reported Oct 26, 2022

Tuscan Garden Restaurant Style Italian Dressing , Net 16 FL OZ (1 PT) 473 mL, Plastic Bottle 12 count mixed case…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Treehouse Foods

FDA (openFDA food enforcement)

Medical devices

Reported Oct 19, 2022

Veritas Advanced Infusion Packs. Used in ophthalmic procedures.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Johnson & Johnson Surgical Vision, Inc.

FDA (openFDA device enforcement)

Food

Reported Oct 12, 2022

Sprigs - Dental Health: Herbal Dietary Supplement 8oz glass amber bottles with black dropper, 12 units per case

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Eden's Answers Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Oct 12, 2022

Fila Manila Coconut Jam NET WT. 12 OZ (340g) UPC:860003619353

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Fila Manila Corporation

FDA (openFDA food enforcement)

Medical devices

Reported Oct 12, 2022

MR Patient Care Portal 5000 (Desktop Unit), Model Number 453564792561 This is a component of product number 866162.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips North America LLC

FDA (openFDA device enforcement)

Medical devices

Reported Oct 12, 2022

Philips Respironics Amara View Minimal Contact Full-Face Mask

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Philips Respironics, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 12, 2022

WFM 365 Organic Creamy Caesar, 12oz, UPC#: 99482490029, Keep Refrigerated. Bottled in USA. Distributed by: Whole Foods…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Vanlaw Food Products, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Oct 5, 2022

VIDAS CMV IgM, 30 tests, REF 30205-01, IVD, Rx.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

bioMerieux, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 5, 2022

BD Pyxis MedBank Cabinet Software v2.1.2.9 Legacy MedBank Cabinets with Matrix Drawers include: . CUBEX MedFlex…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 5, 2022

Collagen Dental Wound Dressing - Bovine Dermis Tap, 25mm x 75mm Product was distributed under the following brand…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Collagen Matrix Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 5, 2022

Ambra PACS, Ambra ProViewer. Software for use as a primary diagnostic and analysis tool for diagnostic images.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

DICOM Grid, Inc. d/b/a Ambra Health

FDA (openFDA device enforcement)

Medical devices

Reported Oct 5, 2022

MEDLINE CLEARPRO DOUBLE SWIVEL CLOSED SUCTION CATHETER, flat peel pouch EA, 10 EA per Inner Carton (IC), 20 EA/2 Inner…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

MEDLINE INDUSTRIES, LP - Northfield

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 5, 2022

OSSUR Power Knee REF PKA10003 OSSUR Power Knee REF PKA10003 OSSUR Power Knee REF PKA01001L OSSUR Power Knee REF…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ossur Americas

FDA (openFDA device enforcement)

Medical devices

Reported Oct 5, 2022

t:slim X2 insulin pump; t:slim X2 insulin pump with Dexcom G5; t:slim X2 insulin pump with Basal-IQ technology; t: slim…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Tandem Diabetes Care Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 28, 2022

BD MaxGuard Extension Set with 4-way stopcock, REF: M4058

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Carefusion

8 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 28, 2022

AquaC UNO H [120V, 60Hz, 1000VA, US-Version - a reverse osmosis unit intended for use with hemodialysis systems.…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Fresenius Medical Care Holdings, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 28, 2022

Grappler Suture Anchor, Titanium, 3.0 x 10mm, Sterile Kit, REF: P44-110-3010-SK, for use within the Grappler Suture…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Paragon 28, Inc.

FDA (openFDA device enforcement)

Free recall alerts

Get alerted about new Indiana recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Other states

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.