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Abbott Laboratories

Abbott Laboratories Recalls

All product recalls associated with Abbott Laboratories.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

143

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 5041–5060 of 37665 recalls

ARCHITECT c4000 Processing Module (Abbott) – undeclared latex (2023)

The devices contain a dry natural rubber (latex) subcomponent, which are not labeled as containing dry natural rubber(latex).

Moderate

FDAOct 19, 2023AL, AK, AZ +45 more• Abbott Laboratories

Combo Kit (Integra) – packaging defect (2023)

Defect in the outer packaging of the Cranial Access Kits. can cause the packaging to split without any additional forces outside compromising the sterility of the device

High

FDAOct 19, 2023Nationwide• Integra LifeSciences Corp.

Cranial Access Kit (Integra) – packaging defect (2023)

Defect in the outer packaging of the Cranial Access Kits can cause the packaging to split without any additional forces outside compromising the sterility of the device

High

FDA

1...251 252253254 255...1884

Page 253 of 1884Next

Oct 19, 2023

Nationwide

• Integra LifeSciences Corp.

Cranial Access Kit (Integra) – packaging defect (2023)

Defect in the outer packaging of the Cranial Access Kits can cause the packaging to split without any additional forces outside compromising the sterility of the device

High

FDAOct 19, 2023Nationwide• Integra LifeSciences Corp.

Leg Bag (Medline) – undeclared latex (2023)

Undeclared Allergen

Undeclared latex

Moderate

FDAOct 19, 2023Nationwide• MEDLINE INDUSTRIES, LP Northfield

Collard Greens (Kroger) – Listeria Contamination (2023)

Listeria

Potential contamination of Listeria monocytogenes

Class IHigh

FDAOct 19, 2023AL, AR, GA +7 more• The Kroger Co

Alinity c Processing Module (Abbott) – undeclared latex (2023)

The devices contain a dry natural rubber (latex) subcomponent, which are not labeled as containing dry natural rubber(latex).

Moderate

FDAOct 19, 2023AL, AK, AZ +45 more• Abbott Laboratories

Dark Chocolate Chip Waffles (Nature's Path) – Undeclared Peanut (2023)

Undeclared Nuts

undeclared peanut

Class IIModerate

FDAOct 19, 2023CA, CO, CT +14 more• Nature'S Path Foods Inc

Pumpkin Spice Waffles (Nature's Path) – Undeclared Peanut (2023)

Undeclared Nuts

undeclared peanut

Class IIModerate

FDAOct 19, 2023CA, CO, CT +14 more• Nature'S Path Foods Inc

Leg Bag (Medline) – undeclared latex (2023)

Undeclared Allergen

Undeclared latex

Moderate

FDAOct 19, 2023Nationwide• MEDLINE INDUSTRIES, LP Northfield

Alinity i Processing Module (Abbott) – undeclared latex (2023)

The devices contain a dry natural rubber (latex) subcomponent, which are not labeled as containing dry natural rubber(latex).

Moderate

FDAOct 19, 2023AL, AK, AZ +45 more• Abbott Laboratories

Biochem HSC 70-LV Sanitizer (Integrity) – Chemical Levels (2023)

CGMP Deviation: Third party test results showing a presence of acetal and acetaldehyde at levels above USP specified amounts.

Class IIModerate

FDAOct 18, 2023IN, OK• Integrity Bio-Chemicals LLC

Biochem HSC 70-LM Sanitizer (Integrity) – Chemical Levels (2023)

CGMP Deviation: Third party test results showing a presence of acetal and acetaldehyde at levels above USP specified amounts.

Class IIModerate

FDAOct 18, 2023IN, OK• Integrity Bio-Chemicals LLC

Biochem HSC 70-VA Sanitizer (Integrity) – Chemical Levels (2023)

CGMP Deviation: Third party test results showing a presence of acetal and acetaldehyde at levels above USP specified amounts.

Class IIModerate

FDAOct 18, 2023IN, OK• Integrity Bio-Chemicals LLC

Blueberry Buckwheat Waffles (Treehouse) – Peanut Contamination (2023)

potentially contaminated with peanut

Class IIILow

FDAOct 18, 2023CA, IL, IA +2 more• Treehouse Foods

Proterra Catalyst (Proterra) – electrical system issue (2023)

Proterra Operating Company, Inc. (Proterra) is recalling certain 2019-2022 40' and 35' Catalyst 800V transit buses equipped with ProDrive 1.0, and 40' and 35' ZX5 800V transit buses equipped with ProDrive 1.0. A transistor inside the inverter may overheat and fail, which can result in a loss of power steering and drive power.

High

NHTSAOct 17, 2023Nationwide• PROTERRA

SagiPlan 2.2 (Bebig) – measurement accuracy issue (2023)

Due to software malfunction, numerical values may be rounded resulting in inaccurate measurements.

Low

FDAOct 17, 2023MD• Bebig Isotopentechnik Gmbh Robert-Rossle-Str. 10 Berlin Germany

PCF-H190DL Colonovideoscope (Aizu Olympus) – repair defect (2023)

Specific devices may have an improperly repaired light guide connector due to missing adhesive to secure the suction channel mouthpiece to the scope connector. Issue may result in loss of image, decreased suction, or impact the ability to effectively reprocess the device. This in turn may lead to unanticipated delay to treatment, or patient exposure to contaminated material and subsequent infection.

High

FDAOct 16, 2023FL, KY, MA +3 more• Aizu Olympus Co., Ltd. 3 Chome 1-1 Niiderakita Aizuwakamatsu Japan

Storyteller Overland Mode LT (Storyteller) – labeling issue (2023)

Storyteller Overland is recalling certain 2022-2023 Ford Transit Storyteller Mode LT motorhomes. The tire and loading information label may indicate an incorrect tire size and pressure. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 110, "Tire Selection and Rims."

High

NHTSAOct 16, 2023Nationwide• STORYTELLER OVERLAND

PCF-H190L Colonovideoscope (Aizu Olympus) – repair defect (2023)

High

FDAOct 16, 2023FL, KY, MA +3 more• Aizu Olympus Co., Ltd. 3 Chome 1-1 Niiderakita Aizuwakamatsu Japan