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.
Reported Aug 28, 2019
ABL90 FLEX Analyzer REF 393090 UDI:05700693930909
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer America Inc.
FDA (openFDA device enforcement)
Reported Aug 28, 2019
ACUSON NX2 Diagnostic Ultrasound System, Model # 11284381, RX Only, Siemens Medical Solutions, containing software…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 28, 2019
PRIVATE SELECTION FROZEN TRIPLE BERRY MEDLEY, 48 oz
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Kroger Co.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 21, 2019
Entenmann's Little Bites Soft Baked Cookies (5 pack Mini Chocolate Chip variety) Net Weight of 5ct box 6.88oz. 5…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BIMBO Bakeries USA Inc.
FDA (openFDA food enforcement)
Reported Aug 21, 2019
Aries Bordetella Assay, REF 50-10037, UDI # 00840487101452
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Luminex Corporation
6 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 14, 2019
14F x 20CM SLX Double Lumen Full Tray Hemodialysis catheter insertion kits, Item No. MC061423 Product Usage: An aid for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medical Components, Inc. dba MedComp
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 14, 2019
SmartRelease Endoscopic Carpal Tunnel Release Handpiece (ECTR handpiece), part numbers 81014 and 83014
Moderate riskThis product could cause temporary or reversible health problems — stop using it.MicroAire Surgical Instruments, LLC
FDA (openFDA device enforcement)
Reported Aug 14, 2019
Dimension¿ Ferritin (FERR) Flex¿ reagent cartridge DM FERR Product Usage: The FERR Flex reagent cartridge is intended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Aug 14, 2019
Shirakiku FISH CAKE IWASHI TEN SK F 20/150 g; Net WT. 5.29 oz. Keep frozen, 7 pcs. UPC 074410925246 Distributed by…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Wismettac Asian Foods, Inc.
7 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 9, 2019
Taylor Farms Illinois Inc. Recalls Chicken Products due to Possible Processing Defect
High riskUsing this product could cause serious injury, illness or death — stop using it now.Taylor Farms Illinois, Inc.
USDA FSIS
Reported Aug 7, 2019
Flexible Drill Shaft, FMP Acetabular System Instrumentation REF 803-05-239 RX Encore Medical, L.P.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Encore Medical, LP
FDA (openFDA device enforcement)
Reported Aug 7, 2019
Maximum Pelvic Trainer (MPT)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ralston Group
FDA (openFDA device enforcement)
Reported Aug 7, 2019
Nasal Alar SpO2 Sensor, Adult/Pediatric SpO2 Sensor, Rx Only Product Usage: The Assurance¿ Nasal Alar SpO2 Sensor is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Xhale Assurance, Inc.
FDA (openFDA device enforcement)
Reported Jul 31, 2019
ARCHITECT BNP Calibrators Ptoduct Usage: The ARCHITECT BNP Calibrators are for the calibration of the ARCHITECT iSystem…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Abbott Laboratories
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 31, 2019
BBQ Bread & Pull-A-Part BBQ Bread sold under the brand names of Flowers UPC 7 22500 40792, Ingles UPC 8 68540 15348 &…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Flowers Foods
11 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 31, 2019
Breast Milk Transfer Lid for use with Oral Syringe Connectors Model: 90003S-100
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Medela Inc.
FDA (openFDA device enforcement)
Reported Jul 31, 2019
Merge PACS versions 7.3, 7.3.1, 8.0 and 8.0.1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 31, 2019
Ragu Chunky Sauce Tomato, Garlic & Onion 45oz and 66oz retail sizes sold in plastic jars
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mizkan America, Inc. - Corporate
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 31, 2019
Salmon (Cut)
High riskUsing this product could cause serious injury, illness or death — stop using it now.Topway Enterprises, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jul 24, 2019
Alaris Pump, Model 8100, with bezel mechanical assemblies manufactured with FR-110 plastic resin. The following…
High riskUsing this product could cause serious injury, illness or death — stop using it now.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Jul 24, 2019
Lay' Lightly Salted Barbecue Flavored Potato Chips Net Wt. 7 3/4 OZ. UPC Code 2840063242
High riskUsing this product could cause serious injury, illness or death — stop using it now.Frito-Lay, Inc.
FDA (openFDA food enforcement)
Reported Jul 24, 2019
Anti-fog solution packaged in a Tyvek peel pouch and it is placed into various kits. Kit are labeled as follows:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries, Inc.
FDA (openFDA device enforcement)
Reported Jul 20, 2019
US Foods Retira Productos De Res Y Cerdo Debido A La Posible Contaminación Del Producto
High riskUsing this product could cause serious injury, illness or death — stop using it now.US Foods Inc.
USDA FSIS
Reported Jul 17, 2019
Alaris Pump Infusion Set, Model Codes 10010453, 10010454, 10012144, 10015294, 10015414, 10933805, 11171447, 11404930,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Becton Dickinson & Company
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.