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 Dec 8, 2021

Tastykake Buttercreme Iced Creme Filled Chocolate Cupcakes 14.25oz (6-2ct) box UPC 0 25600 00230 8 & 2.375oz package,…

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)

Medical devices

Reported Dec 8, 2021

GE Centricity Universal Viewer Zero Footprint Client

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 8, 2021

The Steripath Gen2 Blood Collection System Model Number/Description 2700-21-EN / Steripath Gen2 Blood Collection System…

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

Magnolia Medical Technologies, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 8, 2021

NUVASIVE PRECICE Intramedullary Limb Lengthening (IMLL) and (Short) System: Model Number/Item Number/Product…

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

NuVasive Specialized Orthopedics, Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 8, 2021

TK006 Van Krimpet Powder Blend 50#. Item number 4107780

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

Puratos Corporation (HQ and Innovation Center)

19 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 8, 2021

Abbott HeartMate Touch Communication System, REF: HMT1100 (US), HMT1100-R (Rental US), HMT1150 (EU)

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

Thoratec Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 1, 2021

ARCHITECT i1000SR REF 01L86-01/1L86 and 1L87; ARCHITECT i2000SR REF 03M74-02/3M74; ARCHITECT i2000 REF 08C89-01/1G17…

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

Abbott Laboratories

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 1, 2021

BD Nexiva, 20 GA 1.00 IN (1.1 X 25 mm), 3660 ml/hr. 61ml/min; Closed IV Catheter System- Dual port -61 mL/min (3660…

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

Becton Dickinson Infusion Therapy Systems Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 1, 2021

HemosIL ReadiPlasTin (20 mL), Part number 0020301400. An in vitro diagnostic thromboplastin reagent.

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

Instrumentation Laboratory

FDA (openFDA device enforcement)

Medical devices

Reported Dec 1, 2021

Freelite Human Lambda Free Kit (for use on the SPAPLUS) REF LK018.S Freelite Human Lambda Free Kit (for use on the…

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

The Binding Site Group, Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 24, 2021

BIO-RAD BioPlex 2200 REF 12000650 SYPH T PACK Syphilis Total & RPR Reagent Pack The BioPlex Syphilis Total & RPR kit is…

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

Bio-Rad Laboratories, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 24, 2021

SMART FLEX 9x60 BIL, 80cm The S.M.A.R.T.¿ Flex Biliary Stent System is indicated for use in the palliation of malignant…

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

Cordis Corporation

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 24, 2021

Vit Kit-Freeze is intended for use in assisted reproductive procedures for vitrification and storage of human oocytes…

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

Fujifilm Irvine Scientific, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 24, 2021

Sliced Pickled Beets, Net Wt 16oz. (1lb) 454g, packaged under the following brands: 1. Aunt Nellie's, UPC 44300-05463,…

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

Seneca Foods Corporation

FDA (openFDA food enforcement)

Medical devices

Reported Nov 24, 2021

Smith and Nephew EVOS Self-Tapping Locking Screw SST: (1)REF 72413575, 3.5MM x 75MM, and (2) REF 72413570, 3.5MM X…

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

Smith & Nephew, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 24, 2021

Permobil TiLite, Models: Aero Z, and ZRA

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

TiSport, LLC

FDA (openFDA device enforcement)

Drugs

Reported Nov 17, 2021

Cetirizine hydrochloride, 10 mg tablets, 90-count bottle, Distributed by: A-S Medications Solutions, Libertyville, IL…

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

A-S Medication Solutions LLC.

FDA (openFDA drug enforcement)

Medical devices

Reported Nov 17, 2021

Hemodialysis Delivery System, Software Version 2.x.

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

Baxter Healthcare Corporation

FDA (openFDA device enforcement)

Food

Reported Nov 17, 2021

NOW Royal Jelly 1500mg 60 VCAPS UPC 733739025654 NOW Royal Jelly 1500mg 60 VCAPS (Distributed by Sofico) UPC…

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

NOW Health Group Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Nov 17, 2021

Mushroom Stir Fry Blend 9oz container sold individually

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

Taylor Farms Tennessee, Inc.

FDA (openFDA food enforcement)

Food

Reported Nov 17, 2021

Country Oven Cinnamon Roll 4oz, 2.5oz

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

The Kroger Co.

18 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Nov 10, 2021

AY-259-396-6 Nat Chicken (rotisserie) Flavor WONF 18.144kg packages packaged in brown square boxes with blue plastic…

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

Givaudan Flavours Corp.

FDA (openFDA food enforcement)

Food

Reported Nov 10, 2021

Ivar's Kettle Classic Clam Chowder With Uncured Bacon, Item #1952, Costco Item #1270666. The soup is refrigerated and…

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

Ivar's Commissary

FDA (openFDA food enforcement)

Medical devices

Reported Nov 10, 2021

FIVE S 3.5x65, Flexible Intubation Videoscope, REF: 091361-01 (1 Unit), and 091361-06 (6 Units)

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

Karl Storz Endoscopy

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.