All recall categories

Recalls distributed in South Dakota

These notices name South Dakota 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.

1,583 stored notices name South Dakota, reported between Jun 27, 2012 and Nov 11, 2026. A further 48,765 notices were distributed nationwide, so they reach South Dakota too — those are in the archive.

Medical devices

Reported Sep 18, 2019

XP- CR Tibial Tray- Interlok 59mm Item # 195268

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

Zimmer Biomet, Inc.

34 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 11, 2019

Alere Cholestech LDX Analyzer, model # 14-874 containing power supplies with the identifying codes of 1837d and 1843d -…

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

Alere San Diego, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 11, 2019

Alaris EtCO2, Model 8300, UDI: 10885403830013, CareFusion for models 11634567 and 8300ADXeN933

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

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Meat & poultry

Reported Sep 10, 2019

Hy-Vee Fresh Commissary Recalls Ready-To-Eat Beef and Chicken Products Due to Misbranding and Undeclared Allergens

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

Hy-Vee Fresh Commissary

USDA FSIS

Medical devices

Reported Sep 4, 2019

EQUISTREAM LONG-TERM HEMODIALYSIS CATHETER, REF/Product Code:5905190, 14.5 Fr. Alphacurve Catheter with Standard Kit,…

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

Bard Peripheral Vascular Inc.

27 more products in this recall

FDA (openFDA device enforcement)

Medical devices

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)

Food

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)

Medical devices

Reported Aug 21, 2019

iGUIDE System with software build iGuide 2.2.0, 2.2.1, and 2.2.2

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

Elekta, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 14, 2019

IDEAL IMPLANT Structured Breast Implant, saline breast implant, in the following sizes: 210cc, 240cc, 270cc, 300cc,…

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

Ideal Implant Incorporated

FDA (openFDA device enforcement)

Medical devices

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)

Medical devices

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)

Food

Reported Jul 31, 2019

Jelly Belly Licorice Bridge Mix. Net Wt. 9 oz. (85g); 12 individual 3 oz. bags per caddy UPC: 071567981675 Manufactured…

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

Jelly Belly

FDA (openFDA food enforcement)

Medical devices

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)

Food

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)

Medical devices

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)

Medical devices

Reported Jul 17, 2019

Giraffe Infant Radiant Warmer Infant radiant warmers provide infrared heat in a controlled manner to neonates who are…

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

GE Healthcare, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 17, 2019

HAMILTON-G5, with software versions less than or equal to 2.60 The HAMILTON-G5/S1 ventilators are designed for…

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

Hamilton Medical AG

FDA (openFDA device enforcement)

Medical devices

Reported Jul 17, 2019

ColoCARE, Cat. No. 5650, packaged 250 envelopes/box, For In-Vitro Diagnostic Use. The firm name on the label is Helena…

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

Helena Laboratories, Corp.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 10, 2019

Centricity Universal Viewer 6.0 Is a device that displays medical images and data from various imaging sources, and…

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

GE Healthcare, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 10, 2019

Signature Select Avocado Chunks, 12 oz. (340 g) Stand-up pouch Re-sealable, Keep Frozen; UPC 2113009412 Ingredient:…

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

Nature's Touch Frozen Foods (West)

FDA (openFDA food enforcement)

Food

Reported Jul 10, 2019

WOODSTOCK ORGANIC GRILLED RED PEPPER, NET WT 10. OZ, packaged in a plastic packaged marked with UPC Code: 4256301714.…

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

UNFI General Corporate

FDA (openFDA food enforcement)

Medical devices

Reported Jun 19, 2019

IntraClude Intra-Aortic Occlusion Device, REF: ICF100, 10.5 Fr (3.5 mm) X 39.4" (100 cm), Rx Only, Sterile EO The…

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

Edwards Lifesciences, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jun 12, 2019

MRSASelect, IVD, REF 63747, containing 20 plates per package. The MRSASelect is indicated for use in conjunction with…

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 Jun 12, 2019

Leica Cryostats, used to produce frozen sample sections for biological, medical and industrial applications, including…

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

Leica Microsystems, 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.