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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

197

Class I (Serious)

410

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 1681–1700 of 3552 recalls

Tri-Color Coleslaw (Dole) – Salmonella Risk (2019)

Salmonella

Canadian Food Inspection Agency reported finding Salmonella in a sample of Coleslaw with Green and Red Cabbage and Carrots.

Class IHigh

FDADec 2, 2019AK, CA, IN +4 more• Dole Fresh Vegetables Inc

3M Company Health Care Business 3m Center: 3M Durapore Advanced, Surgical Tape, Model Numbers: 1590-...

While the product meets all safety and efficacy criteria, long term exposure of 3M Durapore Advanced Surgical Tape to continuous high moisture clinical applications has not fully met all of 3M s performance expectations. This use environment may cause tape bond failure, leading the tape to not perform as intended. Further, the tape fibers may fray which could be accidentally ingested or aspirated.

FDANov 21, 2019Nationwide• 3M Company Health Care Business 3m Center

RAYSEARCH LABORATORIES AB Sveavagen 9 Stockholm Sweden: RayStation stand-alone software treatment planning system...

1...83 848586 87...178

Page 85 of 178Next

Editing a static arc beam may unexpectedly set the MU of the beam to its initial default value of 200 MU. If the bug is triggered, the dose is invalidated and needs to be recalculated before the plan can be approved or exported.

FDANov 18, 2019Nationwide• RAYSEARCH LABORATORIES AB Sveavagen 9 Stockholm Sweden

Linet Spol. S.r.o. Zelevcice 5 Slany Czech Republic: Eleganza 5 (AC powered adjustable bed), Item Numbers: a)...

A component used within the side rail mechanism may malfunction, resulting in the side rail either not locking properly in the upper position or the side rail becoming stuck in the upper position.

FDANov 13, 2019Nationwide• Linet Spol. S.r.o. Zelevcice 5 Slany Czech Republic

Formoterol Budesonide Inhalation (Conversio) – Processing Controls (2019)

Lack of Processing Controls

Class IIModerate

FDANov 12, 2019Nationwide• Integrated Health Concepts Inc. dba Conversio Health

Albuterol Ipratropium Inhalation (Conversio) – Processing Controls (2019)

Lack of Processing Controls

Class IIModerate

FDANov 12, 2019Nationwide• Integrated Health Concepts Inc. dba Conversio Health

Albuterol Ipratropium Triamcinolone (Conversio Health) – Processing Controls (2019)

Lack of Processing Controls

Class IIModerate

FDANov 12, 2019Nationwide• Integrated Health Concepts Inc. dba Conversio Health

Albuterol Budesonide Inhaler (Conversio Health) – Processing Controls (2019)

Lack of Processing Controls

Class IIModerate

FDANov 12, 2019Nationwide• Integrated Health Concepts Inc. dba Conversio Health

Albuterol Ipratropium (Conversio Health) – Processing Controls (2019)

Lack of Processing Controls

Class IIModerate

FDANov 12, 2019Nationwide• Integrated Health Concepts Inc. dba Conversio Health

Budesonide Inhalation Vial (Conversio) – Processing Controls (2019)

Lack of Processing Controls

Class IIModerate

FDANov 12, 2019Nationwide• Integrated Health Concepts Inc. dba Conversio Health

Abbott Gmbh & Co. KG Max-Planck-Ring 2 65205 Wiesbaden Germany: ARCHITECT HAVAB-G Calibrator, REF 6L27-01

Abbott has identified that Calibrator lot 08219BE00 is potentially impacted by an increase in Relative Light Units (RLUs) up to 94%. It has been confirmed that the increase in the calibrator RLU values may cause a decrease in the control values and patient results. Patient values generated using the impacted calibrator lot 08219BE00 may have changed interpretation from reactive to falsely non reactive. Results impacted may present as a (falsely) non reactive result that fall in the range between 0.50 to 0.99 S/CO.

FDANov 7, 2019AZ, CA, CO +20 more• Abbott Gmbh & Co. KG Max-Planck-Ring 2 65205 Wiesbaden Germany

The Binding Site Group, Ltd.: Rheumatoid Factor (RF) Kit for use on SPAPLUS, for in-vit...

It has been identified that the rheumatoid factor (RF) calibrator values over recover in comparison to the reference material RF serum. This could result in reporting falsely abnormal results which may lead to unnecessary additional serological testing.

FDANov 6, 2019CA, IN• The Binding Site Group, Ltd.

Abbott GmBH & Co. KG Max-Planck-Ring 2 65205 Wiesbaden Germany: Alinity c Carbon Dioxide Reagent Kit, Produced for Abbot...

Abbott internal studies have determined that atmospheric Carbon Dioxide (CO2) can be absorbed into the Alinity c Carbon Dioxide reagent, resulting in the potential for incorrect results. Abbott was made aware of this issue from customer complaints. Internal testing demonstrated that the amount of CO2 absorbed is higher with increased reagent carousel rotation and when the volume of reagent in the cartridge is reduced. This phenomenon can be detected as a shift in QC. The shift is predictive in both direction and magnitude of the potential impact to patient results.

FDAOct 23, 2019Nationwide• Abbott GmBH & Co. KG Max-Planck-Ring 2 65205 Wiesbaden Germany

PF-Succinylcholine Chloride (Nephron) – Incorrect Labeling (2019)

Incorrect labeling: Incorrect or missing lot and/or exp date

Class IIILow

FDAOct 21, 2019Nationwide• Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center

Taewoong Medical Co., Ltd. 14 Gojeong-ro, Wolgot-Myeon, Gimpo-Si, Gyeonggi-Do Korea (the Republic of): Niti-S Esophageal Stent, REF ES1806F, ES1808F, ES1810F, E...

Misprinted IFUs shipped with esophageal stents

FDAOct 18, 2019IN• Taewoong Medical Co., Ltd. 14 Gojeong-ro, Wolgot-Myeon, Gimpo-Si, Gyeonggi-Do Korea (the Republic of)

Smooth & Creamy Take the Cake Ice Cream (Harris Teeter) – undeclared soy (2019)

The firm discovered that the allergen soy was not declared in the ingredient statement or allergen declaration.

Class IIModerate

FDAOct 17, 2019AL, NC, VA• Harris Teeter Supermarkets, LLC dba Hunter Farms

Harris Teeter Chocolate Ice Cream – Undeclared Soy (2019)

The firm discovered that the allergen soy was not declared in the ingredient statement or allergen declaration.

Class IIModerate

FDAOct 17, 2019AL, NC, VA• Harris Teeter Supermarkets, LLC dba Hunter Farms

Fresh Market Mint Chip Ice Cream (Harris Teeter) – undeclared soy (2019)

The firm discovered that the allergen soy was not declared in the ingredient statement or allergen declaration.

Class IIModerate

FDAOct 17, 2019AL, NC, VA• Harris Teeter Supermarkets, LLC dba Hunter Farms

Mint Chocolate Chip Ice Cream (Harris Teeter) – undeclared soy (2019)

The firm discovered that the allergen soy was not declared in the ingredient statement or allergen declaration.

Class IIModerate

FDAOct 17, 2019AL, NC, VA• Harris Teeter Supermarkets, LLC dba Hunter Farms

Signature Orthopaedics Europe Ltd Unit A, IDA Business & Technology Park Garrycastle Athlone Ireland: Encina HA Femoral Stem, Size 11 Coxa Vara Collared, REF 1...

The firm has identified that packaging containing components of the hip replacement range are mislabeled. This could result in the product intended to be used for a procedure not included in the packaging resulting in a surgical delay.

FDAOct 9, 2019CA• Signature Orthopaedics Europe Ltd Unit A, IDA Business & Technology Park Garrycastle Athlone Ireland