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Dole Fresh Vegetables Inc

Dole Fresh Vegetables Inc Recalls

All product recalls associated with Dole Fresh Vegetables Inc.

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Recall Summary

Total Recalls

1000

Past Year

423

Class I (Serious)

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 1661–1680 of 4598 recalls

Dole Sesame Asian Chopped Salad Kit – Undeclared Egg (2021)

Undeclared Allergen

Incorrect product master-pack label causing an undeclared allergen; egg.

Class IHigh

FDAJan 5, 2021AK, CA, ID +6 more• Dole Fresh Vegetables Inc

Oxycodone Oral Solution (Genus) – Foreign Substance (2020)

Presence of Foreign Substance: Particulate matter was found in multiple lots of product.

Class IIILow

FDADec 23, 2020Nationwide• Genus Lifesciences Inc.

Cytocell Ltd. 418 Cambridge Science Park, Milton Road Oxford Gene Technology Cambridge United Kingdom: Aquarius LPH 511-A CRLF2 Distal Probe Green, model no. LP...

Users may observe very faint additional locus specific signals at 11q13. There is a low risk of a normal sample being reported as not normal in a resulting laboratory developed test (LDT) that utilizes the LPH511-A CRLF2 Distal Probe Green.

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FDADec 22, 2020CA, IL, MI +4 more• Cytocell Ltd. 418 Cambridge Science Park, Milton Road Oxford Gene Technology Cambridge United Kingdom

Epinephrine/Lidocaine Solution (Edge) – Incorrect Labeling (2020)

Labeling: Incorrect or Missing Lot and/or Exp Date

Class IIILow

FDADec 22, 2020PA• Edge Pharma, LLC

Vegan Chocolate Cake (Gem City Fine Foods) – Mislabeled Nutrition Facts (2020)

Mislabeled - Nutrition facts panel and list of ingredients were incorrect.

Class IIModerate

FDADec 22, 2020IN, TX• Gem City Fine Foods, LLC

Getinge Group Logistics America, LLC: Getinge CM320 Series Washer Disinfector - Product Usage: ...

Fire/Burn Risk

The potential that the plastic inlet hose connections may deform or break as a result of material fatigue and/or over tightening of the clamps. A broken hose connection may lead to a hazardous situation of water leakage or water spray. The water leakage or water spray may result in a burn to the user and/or an inconvenience due to a procedural delay if the Washer Disinfector is taken out of service.

FDADec 21, 2020Nationwide• Getinge Group Logistics America, LLC

GE Healthcare, LLC: System, X-Ray, Tomography, Computed: Revolution Apex, Rev...

Laceration Risk

GE Healthcare has become aware of a potential issue on Revolution Apex, Revolution CT with Apex Edition, Revolution CT, and Revolution CT ES systems where the table pinch protector could be damaged or missing leading to exposed table screws which could cause a laceration due to a sharp edge.

FDADec 17, 2020Nationwide• GE Healthcare, LLC

2014 VOLKSWAGEN BEETLE CONVERTIBLE Recall: AIR BAGS:FRONTAL

Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2012-2014 Volkswagen Beetle and Beetle Convertible vehicles. The driver's side air bag inflator may explode due to propellant degradation occurring after long-term exposure to high absolute humidity, high temperatures, and high temperature cycling.

NHTSADec 16, 2020Nationwide• VOLKSWAGEN

Medtronic Neurosurgery: REF 27219-2 X1, Medtronic, Delta Valve, Neonatal, Perfor...

Neonatal Valves were manufactured with a ventricular catheter connection site shorter than the design specification. The defect can lead to difficulty in securing the valve to the proximal catheter which could result in disconnection of the ventricular catheter from the valve and shunt malfunction

FDADec 16, 2020Nationwide• Medtronic Neurosurgery

Medtronic Neurosurgery: REF 27219-1 X1, Medtronic, Delta Valve, Neonatal, Perfor...

FDADec 16, 2020Nationwide• Medtronic Neurosurgery

Medtronic Neurosurgery: REF 27219-5 X1, Medtronic, Delta Valve, Neonatal, Perfor...

FDADec 16, 2020Nationwide• Medtronic Neurosurgery

Qiagen Sciences LLC: therascreen PIK3CA RGQ PCR Kit (23) US IVD product- aid c...

Kit may generate false Q546R mutation positive results caused by nonspecific molecular interactions within the Q546R higher than previously observed and described within the Instructions For Use.

FDADec 11, 2020CA, IN, MI +6 more• Qiagen Sciences LLC

Homfa Cabinets (Shenzhen Luosi Ge) – Tip-Over Risk (2020)

This recall involves the Homfa HPB-087 and HPB-106 cabinets. The HPB-087 was sold in walnut brown and the HPB-106 was sold in wood grain. The cabinets measure about 29.75 inches tall, 31.5 inches wide, and 15.4 inches deep and weigh about 59 pounds.

CPSCDec 10, 2020Nationwide• Shenzhen Luosi Ge Trading Co., of China (owner of Homfa trademark)