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.

4,309 stored notices name Indiana, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,784 notices were distributed nationwide, so they reach Indiana too — those are in the archive.

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)

Medical devices

Reported Sep 21, 2022

MicroClave Clear Neutral Connector. A bidirectional connector used as an accessory to an intravascular catheter placed…

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

ICU Medical, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 21, 2022

Capri Sun, Wild Cherry, Flavored Juice Drink Blend in 6floz. foil pouch. Sold in carton containing 10 pouches. Carton…

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

Kraft Heinz Foods Company

FDA (openFDA food enforcement)

Medical devices

Reported Sep 21, 2022

Verify SixCess Challenge Pack. Used to confirm that critical parameters of steam sterilization have been reached within…

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

Steris Corporation Hopkins Facility

FDA (openFDA device enforcement)

Medical devices

Reported Sep 14, 2022

CARTO VIZIGO 8.5F Bi-Directional Guiding Sheath, REF: D138501. Used to introduce various cardiovascular catheters into…

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

Biosense Webster, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 14, 2022

Product Description/Item: ChemoLock Bag Spike, 10 units/CL-10-10; ChemoLock BAG SPIKE w/ ADDITIVE PORT, DRY…

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

ICU Medical, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 14, 2022

Starbucks Vanilla Espresso Triple Shot, 15 oz, 12 bottles per case.

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

Pepsico Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 14, 2022

Philips BiPAP A30, Rx Only. To provide noninvasive ventilation support for patients with obstructive sleep apnea…

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

Philips Respironics, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Drugs

Reported Sep 7, 2022

Colgate Anticavity Fluoride Toothpaste, OPTIC WHITE PRO SERIES, Stain Prevention, 5% Hydrogen Peroxide, Net Wt. 2.1 OZ.…

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

Family Dollar Stores, Llc.

5 more products in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Sep 7, 2022

T-SPOT.TB REF TB.300 US

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

Oxford Immunotec Ltd.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 7, 2022

therascreen FGFR RGQ RT-PCR kit (US IVD) REF 874721

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

Qiagen Sciences LLC

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 7, 2022

Woodland Ingredients X06D Arborio Rice, 25 lbs. bag UPC 00687080007374 Woodland Ingredients X16D Italian Arborio Rice,…

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

Woodland Foods LLC

FDA (openFDA food enforcement)

Food

Reported Sep 7, 2022

Priyems Sambar Spicy Lentil Soup 800 grams (1.76 lbs) UPC 8 61754 00010 0, 8 retail units per wholesale case, Frozen

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

Yem Foods LLC

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 31, 2022

NUCLISENS easyMAG Magnetic Silica, REF 280133, 24 x 1.2mL bottles/kit.

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

bioMerieux, Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 31, 2022

Organic Amaranth Grain Gluten Free, Bob's Red Mill brand, packaged in Standup Pouch (24oz). Each case consists of 4/24…

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

Bob's Red Mill Natural Foods, Inc.

FDA (openFDA food enforcement)

Food

Reported Aug 31, 2022

Capriole Goat Cheese, Fresh Goat Cheese, Wasabi 5 pound and 8oz logs

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

Capriole, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 31, 2022

DeRoyal limb holders: (1) DeRoyal Limb Holder, Wrist, Fixed, Quick Release, REF M8124; (2) DeRoyal Limb Holder, Ankle,…

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

DeRoyal Industries Inc.

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.