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Recalls distributed in Mississippi

These notices name Mississippi 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.

2,512 stored notices name Mississippi, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,784 notices were distributed nationwide, so they reach Mississippi too — those are in the archive.

Medical devices

Reported Apr 4, 2018

(1) Sigma HP Cemented Trochlea Size 1 Narrow Left, Catalog Number: 102403100, GTIN: 10603295001614; (2) Sigma HP…

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

DePuy Orthopaedics, Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 4, 2018

Product Name Lot Number or ID Whiskey & Cola Type Flavored Seasoning 660373

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

Griffith Foods

7 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Apr 4, 2018

Sonimage HS1 Ultrasound Kit AC adapter, Product Number: A7AP, UDI: 04560141940031

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

Konica Minolta Medical Imaging USA, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 4, 2018

Gas Module 3 monitoring spirometer, Part Number: 115-030108-00 Product Usage: The Gas Module 3 is an accessory device…

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

Mindray DS USA, Inc. dba Mindray North America

FDA (openFDA device enforcement)

Food

Reported Apr 4, 2018

Southgate Hot Dog Chili Sauce 15 oz cans UPC 0 71846 95242

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

Vietti Acquisitions, LLC

FDA (openFDA food enforcement)

Meat & poultry

Reported Mar 31, 2018

PFP Enterprises LLC Retira Productos De Carne De Res Cruda Producidos Sin El Beneficio De La Inspeccin

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

Patterson TMP Operating, LLC

USDA FSIS

Medical devices

Reported Mar 28, 2018

Malecot Nephrostomy Catheter System, Product Number: M001224110, GTIN: 08714729030980 The Malecot and the Stenting…

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

Boston Scientific Corporation

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 28, 2018

CATHETER REPAIR KIT, REF AAC52001, UDI 884908001891 Product Usage: The Medcomp Repair Kit is indicated for use in…

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

Medical Components, Inc. dba MedComp

9 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 21, 2018

NovaKone Daily Wear Soft contact; Catalog Number: AONKS54 Product Usage: The NOVAKONE SPHERICAL lens is indicated for…

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

Alden Optical

10 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 21, 2018

OneStep CPR Complete, Adult Multi Function Electrodes, Part Numbers: 8900 0214 01 (case of 8 single electrodes, UDI:…

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

ZOLL Medical Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Mar 14, 2018

i-STAT DE handheld data processing module for clinical use, Software Version 2.8, List Number:08K46-01115200 (UDI:…

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

Abbott Point Of Care Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 14, 2018

Medtronic Synchromed II Model 8637 supplied in 20mL and 40 mL reservoir size and a catheter. Product Usage: The…

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

Medtronic Neuromodulation

FDA (openFDA device enforcement)

Medical devices

Reported Mar 14, 2018

2.5 mm Reaming Rod, Ball tip, 950 mm, sterile, Part Number: 351.706S Reaming Rods are intended for guiding of reamers…

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

Synthes (USA) Products LLC

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 7, 2018

STAT 2¿ I.V. Gravity Flow Controller and STAT 2¿ Primary, Secondary Administration Sets and Extension Sets (Catalog…

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

ConMed Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 7, 2018

Agility with Integrity R3.2

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

Elekta Limited

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 7, 2018

Footswitch accessory to the CUSA Clarity Ultrasonic Tissue Ablation System; Catalogue No: C7000 Product Usage: The…

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

Integra LifeSciences Corp.

FDA (openFDA device enforcement)

Food

Reported Mar 7, 2018

Seggiano Artichoke & Garlic Sauce & Spread Net Weight 200g, 7.1 oz, packaged in Glass jar, UPC Code: 812603020381

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

Seggiano USA Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Mar 7, 2018

ST AIA-PACK¿ PROG II, Progesterone II Assay, Part Number: 025239

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

Tosoh Bioscience Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 28, 2018

Innova Self-Expanding Stent System, 200 mm. Labeled with Material Number and description as follows: Product Usage: The…

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

Boston Scientific Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 28, 2018

Frozen Unbaked Biscuits sold under the brand names of Hilltop Hearth, Mary B's & Marshall.

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

Holsum Baking Company Warehouse

FDA (openFDA food enforcement)

Food

Reported Feb 28, 2018

IQF Green beans, sold as Not Ready To Eat (NRTE) product for use in foodservice or manufacturing applications. The…

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

National Frozen Foods Corporation--Seattle

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 28, 2018

Pentax Video Duodenoscope Model: ED-3490TK (UDI of design being recalled: 04961333232420) These instruments are…

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

Pentax

FDA (openFDA device enforcement)

Medical devices

Reported Feb 21, 2018

Carestation 620 A1, Carestation 650 A1, and Carestation 650c A1

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

GE Medical Systems China Co., Ltd.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 21, 2018

Blastomyces dermatitidis Antiserum 1 mL vial GIBSON BIOSCIENCE. Catalog 200265 Intended for identification of the…

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

Gibson Laboratories LLC

FDA (openFDA device enforcement)

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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.