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Rancho Santo Cristo, Inc

Rancho Santo Cristo, Inc Recalls

All product recalls associated with Rancho Santo Cristo, Inc.

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Recall Summary

Total Recalls

1000

Past Year

88

Class I (Serious)

98

Most Recent

Nov 2025

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 161–180 of 2399 recalls

SAVPAK Duro 10x10 8oz (Rancho Santo Cristo) – Wheat allergen (2024)

Undeclared Allergen

Undeclared Wheat Allergen

FDAJun 12, 2024TX• Rancho Santo Cristo, Inc

Fresenius Blood Pump Rotor (Fresenius) – Dislodgement Risk (2024)

An increased number of complaints were reported on the Blood Pump Rotor (P/N - F40015481 REV A) after a period of use by clinics noting loose/dislodged guide sheaves.

FDAJun 3, 2024Nationwide• Fresenius Medical Care Holdings, Inc.

Fresenius Blood Pump Rotor (Fresenius) – Dislodgement Risk (2024)

An increased number of complaints were reported on the Blood Pump Rotor (P/N - F40015481 REV A) after a period of use by clinics noting loose/dislodged guide sheaves.

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FDAJun 3, 2024Nationwide• Fresenius Medical Care Holdings, Inc.

Fresenius Blood Pump Rotor (Fresenius) – Dislodgement Risk (2024)

An increased number of complaints were reported on the Blood Pump Rotor (P/N - F40015481 REV A) after a period of use by clinics noting loose/dislodged guide sheaves.

FDAJun 3, 2024Nationwide• Fresenius Medical Care Holdings, Inc.

Fresenius Blood Pump Rotor (Fresenius) – Dislodgement Risk (2024)

An increased number of complaints were reported on the Blood Pump Rotor (P/N - F40015481 REV A) after a period of use by clinics noting loose/dislodged guide sheaves.

FDAJun 3, 2024Nationwide• Fresenius Medical Care Holdings, Inc.

Fresenius Blood Pump Rotor (Fresenius) – Dislodgement Risk (2024)

An increased number of complaints were reported on the Blood Pump Rotor (P/N - F40015481 REV A) after a period of use by clinics noting loose/dislodged guide sheaves.

FDAJun 3, 2024Nationwide• Fresenius Medical Care Holdings, Inc.

Fresenius Blood Pump Rotor (Fresenius) – Dislodgement Risk (2024)

An increased number of complaints were reported on the Blood Pump Rotor (P/N - F40015481 REV A) after a period of use by clinics noting loose/dislodged guide sheaves.

FDAJun 3, 2024Nationwide• Fresenius Medical Care Holdings, Inc.

Fresenius Blood Pump Rotor (Fresenius) – Dislodgement Risk (2024)

An increased number of complaints were reported on the Blood Pump Rotor (P/N - F40015481 REV A) after a period of use by clinics noting loose/dislodged guide sheaves.

FDAJun 3, 2024Nationwide• Fresenius Medical Care Holdings, Inc.

Fresenius Blood Pump Rotor (Fresenius) – Dislodgement Risk (2024)

An increased number of complaints were reported on the Blood Pump Rotor (P/N - F40015481 REV A) after a period of use by clinics noting loose/dislodged guide sheaves.

FDAJun 3, 2024Nationwide• Fresenius Medical Care Holdings, Inc.

Suntegrity Sunscreen (Synchronicity) – CGMP Deviations (2024)

CGMP Deviations

Class IIModerate

FDAMay 24, 2024Nationwide• SYNCHRONICITY SPA INC, DBA SUNTE

Suntegrity Sunscreen (Synchronicity) – Microbial Contamination (2024)

Microbial Contamination of Non-Sterile Products: Presence of Aspergillus Sydowii (Mold)

FDAMay 24, 2024Nationwide• SYNCHRONICITY SPA INC, DBA SUNTE

US AquaA 900H Water Purifier (Fresenius) – Concentrate Flow Error (2024)

Concentrate Flow was exceeding the maximum 19.9 bar set point. The standard default set point range is between 4 and 18.Error message (F020104, "concentrate pressure alarm limit exceeded") concentrate pressure is too high and stops the dialysis water supply.

FDAMay 16, 2024Nationwide• Fresenius Medical Care Holdings, Inc.

Electric Ranges (Frigidaire/Kenmore) – Fire Hazard (2024)

This recall reannouncement involves Frigidaire, Frigidaire Gallery, Frigidaire Professional, and Kenmore Elite smooth-top electric ranges. The smooth-top electric ranges have rear panel rotary knobs and digital displays. They were sold in the following colors: white, bisque, black and stainless steel. The brand name, model, and serial number for each unit are located on the frame of the drawer at the bottom of the unit when the drawer is opened. The following models and serial numbers are included in the recall: Rose Pink, Light Pink, Pure White, Falcon Gray and Green Mist, with Light Blue, Navy, Peacock Blue, Gray Frigidaire Models Model Numbers FEFBZ90GC* FEFLMC55GC* FEFLZ87GC* GLEF396AB* GLEF396AQ* GLEF396AS* GLEF396CQ* GLEF396CS* GLEFM397DB* GLEFM397DQ* GLEFM397DS* GLEFM97FPB* GLEFM97FPW* GLEFM97GPB* GLEFM97GPW* LEEFM389FE* PLEF398AC* PLEF398CC* PLEF398DC* PLEFM399DC* PLEFMZ99EC* PLEFMZ99GC* PLEFZ398EC* PLEFZ398GC* Frigidaire Serial Numbers Serial Number Range VF122xxxxx - VF334xxxxx Kenmore Elite Models Model Numbers 790.990121* 790.990131* 790.990141* 790.990191* Kenmore Elite Serial Numbers Serial Number Range VF122xxxxx - VF334xxxxx

CPSCMay 16, 2024Nationwide• Electrolux Home Products Inc., of Charlotte, North Carolina

Accu-Chek Guide Kit (Roche) – Measurement Unit Error (2024)

The reason for recall is the meters may show an incorrect measurement unit (mmol/L rather than mg/dL) and may result in the wrong unit of measure. Which may subsequently cause an error in interpreting a result as approximately 18 times lower that the actual blood glucose. Potential immediate health consequences of the glucose meter providing a reading in the wrong units of measurement (UOM) may result in inappropriate rescue therapy for presumed hypoglycemia including urgent and repeat administration of carbohydrates. This in turn could lead to frequent episodes of hyperglycemia which is unrecognized and undertreated.Long range consequences of continued use of the affected meters could include mismanagement of the patient s diabetes for longer periods of time potentially resulting in a major health event (in general persistent and/or severe hyperglycemia) that may lead them to seek medical attention, and depending on the duration of hyperglycemia, could contribute to the development of microvascular (i.e., retinopathy, neuropathy, nephropathy) and/or macrovascular (i.e., myocardial infarction, ischemic stroke) complications of diabetes and could lead to fetal damage (abnormal fetal growth and altered organ development and maturation, fetal hypoxemia, spontaneous abortion, and congenital anomalies) in pregnant women. This issue was identified by three initial consumer complaints, with reports that the meters were presenting the incorrect unit of measure.

FDAMay 13, 2024Nationwide• Roche Diabetes Care, Inc.

Kosmos iOS Ultrasound (Echonous) – Measurement Inaccuracy (2024)

Ultrasound system has a bug in affected iOS software, which after DICOM export, can cause inaccuracy in postprocessed measurements done in 3rd party software, such as PACS or other post-processing software, which may lead to inaccurate diagnoses or treatment.

FDAMay 9, 2024AL, AK, AZ +29 more• Echonous Inc

CORI Surgical System (Blue Belt) – Marker Registration Error (2024)

CORI Surgical System with Real Intelligence Software exhibits an increased Marker Registration Error (MRE) which may cause tracker arrays to flicker on screen of the CORI Surgical System during use, and may cause surgical delay

FDAMay 7, 2024Nationwide• Blue Belt Technologies, Inc

Losartan Hydrochlorothiazide (Macleods) – Plastic Contamination (2024)

Presence of foreign substance: plastic-like substance.

Class IIModerate

FDAMay 7, 2024Nationwide• MACLEODS PHARMA USA, INC

Zilretta Injection (Pacira) – Stability Specification Failure (2024)

Failed Stability Specifications - at 12 months 2-8 degrees C followed by 6 weeks at 25 degrees C.

Class IIModerate

FDAMay 7, 2024Nationwide• PACIRA PHARMACEUTICALS INC

EVOLUTION MP Femoral Knee Replacement (MicroPort) – Product Quality (2024)

One confirmed incident has been received that EFSRN4PR, lot number MP1982170, Size 4 Evolution MP Non-Porous Femoral Right was opened during surgery and contained part number EFSRN3PL, lot number MP1982097, Size 3 Evolution MP Non-Porous Femoral Left in the packaging.

FDAMay 3, 2024Nationwide• MicroPort Orthopedics Inc.

Cerene Cryotherapy Device (Channel Medsystems) – Error Code Issue (2024)

Error code 003 was not listed in certain rows of the Device Instructions for Use Troubleshooting section (i.e., Table 22. Summary of LCD Messages and Error Codes).

FDAMay 3, 2024Nationwide• Channel Medsystems, Inc.