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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.

2,477 stored notices name Mississippi, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Mississippi too — those are in the archive.

Medical devices

Reported Sep 27, 2023

Philips Tempus Pro Patient Monitor, REF: 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R, 00-1004, and 00-1007, when Used…

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

Remote Diagnostic Technologies Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 20, 2023

Proclaim XR 5 Implantable Pulse Genterator REF 3660 (previously known as Proclaim" 5 Elite IPG) Model 3660 Product…

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

Abbott Medical

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 20, 2023

FILMARRAY Gastrointestinal (GI) Panel (Part No.: RFIT-ASY-0104 & RFIT-ASY-0116) Pouch Module Software

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

BioFire Diagnostics, LLC

FDA (openFDA device enforcement)

Food

Reported Sep 13, 2023

Nestle Toll House, Chocolate Chip Cookie Dough, 16.5 oz. Cookie dough in bar form packaged in paperboard tray with…

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

Nestle-USA, Inc. (Corporate Office)

FDA (openFDA food enforcement)

Medical devices

Reported Sep 13, 2023

ISee Ortho-K Lens

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

PARAGON VISION SCIENCES, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 13, 2023

Parent's Choice brand Sensitivity Premium Infant Formula, 638g, packaged in plastic tubs; and Tippy Toes brand…

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

PBM Nutritionals, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Sep 6, 2023

Beckman Coulter, IVD, REF: OSR61171, IgA, 4 x 14 mL R1, 4 x 11 mL R2

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

Beckman Coulter Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 30, 2023

Team Fresh & Go: Cantaloupe Cup, packaged in 12oz plastic cup with lid. Packaged and sold as single unit.

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

Freshy Foods, LLC

2 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Aug 9, 2023

Outshine No Sugar Added Strawberry Fruit Bars Brand name: Outshine; Unit size:14.7 fl oz carton with 6 bars; Container…

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

Dreyer's Grand Ice Cream, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 9, 2023

OEC Flexiview 8800 Systems with 9-inch Image Intensifier

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

GE OEC Medical Systems, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 9, 2023

VERITAS Advanced Infusion Packs (VRT-AI) and VERITAS Advanced Fluidics Packs (VRT-AF)

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

Johnson & Johnson Surgical Vision, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 2, 2023

HAMILTON C1 Ventilator REF 161001 1610010 Is intended to provide positive pressure ventilatory support to adults and…

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

Hamilton Medical, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 2, 2023

FRED Flow Re-Direction Endoluminal Device, REF: FRED3507-PMA, FRED3511, FRED3511-PMA, FRED3516-CA, FRED3516-PMA,…

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

Microvention Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 26, 2023

Durepair Dura Regeneration Matrix: DUREPAIR DURA SUBSTITUTE 2 X 2, 61100; DUREPAIR DURA SUBSTITUTE 3 X 3, 61105;…

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

Medtronic Neurosurgery

FDA (openFDA device enforcement)

Food

Reported Jul 26, 2023

Private Selection 48oz Classic Fruit Medley, frozen product, 8/48 oz bags per case. UPC 0 11110 82026 6. Distributed by…

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

Townsend Farms Inc.

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 19, 2023

HeartSine, REF: PAD-PAK-01, PAD-PAK-03 AND PAD-PAK-03j, CE0123 sold separately and with the HeartSine Samaritan Public…

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

HeartSine Technologies Ltd.

FDA (openFDA device enforcement)

Food

Reported Jul 12, 2023

Maggi Masala ae Magic, 6 grams, Packaged in plastic sachets. 1920 sachets per case.

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

Amin Trading Agency LLC

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 12, 2023

BD Pyxis CII Safe, Software: V7, REF: 107-96, 107-97, 107-97-201; BD Pyxis CII Safe, Software: V7, REF: 107-223,…

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

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 12, 2023

da Vinci Xi/X Tip-Up Fenestrated Grasper, REF: 470347, VER: 12

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

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 12, 2023

A20180 BATTER MIX X4 50.00 BAG

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

Newly Weds Foods, Inc.

195 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Jul 12, 2023

Pearl Milling Company Self-Rising Yellow Corn Meal Mix Net Wt 80 oz (5 lb) UPC 3000057380 packaged in paper bag with…

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

PepsiCo Beverages & Foods

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 12, 2023

Quidel Triage Cardiac Panel: REF: 97000HS, 97021HS (Troponin I), 97022HS (CK-MB and Troponin I), 97000HSEU,…

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

Quidel Cardiovascular Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 12, 2023

Aptio Automation Storage and Retrieval Module (SRM)

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

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 28, 2023

Draeger Softbed Resuscitaire and/or Birthing Room Warmer with Scale [Model(s): RW82VHA-1, RW82VHA-1C, RW82VHA-1D,…

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

Draeger Medical Systems, Inc.

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.