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Jenis Splendid Ice Creams LLC

Jenis Splendid Ice Creams LLC Recalls

All product recalls associated with Jenis Splendid Ice Creams LLC.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

127

Most Recent

Jan 2026

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 22641–22660 of 25000 recalls

Sweet Corn with Blackberry (Jenis Splendid) – Unlisted Ingredients (2008)

Frozen desserts do not include ingredients on the labeling.

Class IIModerate

FDAJul 7, 2008Nationwide• Jenis Splendid Ice Creams LLC

Pineapple Yogurt (Jenis Splendid) – undeclared ingredients (2008)

Frozen desserts do not include ingredients on the labeling.

Class IIModerate

FDAJul 7, 2008Nationwide• Jenis Splendid Ice Creams LLC

Goat Cheese with Fig Cognac (Jenis Splendid) – Unlisted Ingredients (2008)

Frozen desserts do not include ingredients on the labeling.

Class II

1...1131 113211331134 1135...1250

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Moderate

FDAJul 7, 2008Nationwide• Jenis Splendid Ice Creams LLC

Backyard Mint Straciatella (Jenis Splendid) – undeclared ingredients (2008)

Frozen desserts do not include ingredients on the labeling.

Class IIModerate

FDAJul 7, 2008Nationwide• Jenis Splendid Ice Creams LLC

Apple Cider Sorbet (Jenis Splendid) – undeclared ingredients (2008)

Frozen desserts do not include ingredients on the labeling.

Class IIModerate

FDAJul 7, 2008Nationwide• Jenis Splendid Ice Creams LLC

Cocoa Zin (Jenis Splendid) – undeclared ingredients (2008)

Frozen desserts do not include ingredients on the labeling.

Class IIModerate

FDAJul 7, 2008Nationwide• Jenis Splendid Ice Creams LLC

Saigon Cinnamon (Jenis Splendid) – Unlisted Ingredients (2008)

Frozen desserts do not include ingredients on the labeling.

Class IIModerate

FDAJul 7, 2008Nationwide• Jenis Splendid Ice Creams LLC

Dark Cocoa Smoked Almond (Jenis Splendid) – undeclared ingredients (2008)

Frozen desserts do not include ingredients on the labeling.

Class IIModerate

FDAJul 7, 2008Nationwide• Jenis Splendid Ice Creams LLC

Integra Pain Management: Radiation Reduction Gloves, sterile, Latex-free, Catalog ...

Radiation reduction gloves were labeled as "Latex-free", but contain natural rubber latex.

FDAJul 7, 2008AL, CA, FL +5 more• Integra Pain Management

Philips Healthcare Informatics, Inc.: Philips Healthcare Informatics iSite PACS (Picture Archi...

Scout line and localizer crosshair on MPR images will display in the incorrect position under certain circumstances.

FDAJul 3, 2008Nationwide• Philips Healthcare Informatics, Inc.

Draeger Medical, Inc.: Evita 4 Critical Care Ventilator. Continuous (Respirator)

audible power failure alarm was not enunciated at the required volume

FDAJul 2, 2008AZ, CA, CO +15 more• Draeger Medical, Inc.

Draeger Medical, Inc.: Evita XL Critical Care Ventilator. Continuous (Respirator)

audible power failure alarm was not enunciated at the required volume

FDAJul 2, 2008AZ, CA, CO +15 more• Draeger Medical, Inc.

Draeger Medical, Inc.: Evita 2 dura Critical Care Ventilator. Continuous (Respir...

Audible power failure alarm was not enunciated at the required volume

FDAJul 2, 2008AZ, CA, CO +15 more• Draeger Medical, Inc.

OEC Medical Systems, Inc: GE OEC 9600 C-arm Fluoroscopy System, GE Healthcare, Surg...

Secondary collimator filters may be missing on certain x-ray units. It was discovered that the secondary collimator filter on some OEC 9600 C-arms was omitted when a collimator assembly was replaced. This would reduce the filtration and therefore the Half-Value-Layer (HVL) of the X-ray beam, and may result in non-compliance with respect to Maximum Entrance Exposure Rate (EER) unless the maximum EE

FDAJul 2, 2008Nationwide• OEC Medical Systems, Inc

SunRinglé Quick Release Devices (Hayes Bicycle) – Fall Hazard (2008)

This recall involves the SunRinglé Hollow Quick Release Devices for bicycles and includes models Hollow CroMo Front 100mm, Hollow CroMo Rear 130mm, and Hollow CroMo Rear 135mm. These devices have hollow skewers. They were sold individually or with SunRinglé front and rear wheels with model names Black Flag, Disc o Flea, Charger, STR8 Track, Accelerator R3.00C and Accelerator T3.0C. "Ringlé" is stamped on the lever. Quick release devices with a solid skewer are not included in this recall.

CPSCJul 2, 2008Nationwide• Hayes Bicycle Group, of Mequon, Wis.

B. Braun Medical, Inc.: Safeline Metriset w/Cassette, inj sties, clamps LL 114 in...

incorrect burette was packaged with the product

FDAJun 30, 2008Nationwide• B. Braun Medical, Inc.

B. Braun Medical, Inc.: Horizon Pump Set w/150 ml burette w/15 um filter and Ultr...

incorrect burette was packaged with the product

FDAJun 30, 2008Nationwide• B. Braun Medical, Inc.

Computerized Medical Systems Inc: Monaco Radiation Treatment Planning System, Monaco Releas...

Monaco: If the user selects Monte Carlo Photon as the Secondary Algorithm (to be used for final dose calculation through segments), and selects SKIP Forward button at any time during stage 2 optimization, the system may only use the pencil beam algorithm for final computation of dose even though Monte Carlo was selected. Other than specific output to the console window, there will be no other in

FDAJun 30, 2008Nationwide• Computerized Medical Systems Inc

B. Braun Medical, Inc.: Metriset Burette Set w/Horizon Pump, Ultrasites, 120 in. ...

incorrect burette was packaged with the product

FDAJun 30, 2008Nationwide• B. Braun Medical, Inc.

B. Braun Medical, Inc.: Add-On Burette Set with 150 ml burette and Ultrasite Inje...

incorrect burette was packaged with the product

FDAJun 30, 2008Nationwide• B. Braun Medical, Inc.