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Abbott GmbH Max-Planck-Ring 2 Wiesbaden Germany

Abbott GmbH Max-Planck-Ring 2 Wiesbaden Germany Recalls

All product recalls associated with Abbott GmbH Max-Planck-Ring 2 Wiesbaden Germany.

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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 4101–4120 of 37665 recalls

Alinity i Anti-HCV Reagent Kit (Abbott) – False Elevated Results (2024)

Customer complaints were received regarding falsely elevated results for some patient samples. Internal studies with customer return samples confirmed potential interactions that may lead to falsely elevated results when processed as below on the same instrument: " ARCHITECT Syphilis TP (LN 8D06) and/or ARCHITECT AdviseDx SARS-CoV-2-IgG II (LN 6S60) precedes ARCHITECT Anti-HCV testing (LN 1L79). " Alinity i Syphilis TP (LN 07P60) precedes Alinity i Anti-HCV testing (LN 08P05).

Low

FDAMar 4, 2024Nationwide• Abbott GmbH Max-Planck-Ring 2 Wiesbaden Germany

X-Guide Handpiece Adaptor Sleeve (X-NAV) – Manufacturing Geometry Defect (2024)

The Handpiece Adaptor may have a manufacturing defect causing incorrect geometry. The incorrect geometry in turn causes the Handpiece Adaptor to not fit onto the doctor's dental handpiece.

Low

FDAMar 4, 2024Nationwide• X-NAV Technologies, LLC

Natural Artesian Water (Fiji) – Bacterial Contamination (2024)

1...204 205206207 208...1884

Page 206 of 1884Next

Firm testing revealed Manganese in addition to three bacterial genera.

Class IIILow

FDAMar 4, 2024Nationwide• Natural Waters of Viti Limited

Febuxostat 80mg (Sun Pharma) – microbial contamination (2024)

CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment.

Class IIModerate

FDAMar 4, 2024Nationwide• SUN PHARMACEUTICAL INDUSTRIES INC

Treprostinil Injection (Par) – particulate matter (2024)

Presence of Particulate Matter.

Class IHigh

FDAMar 4, 2024Nationwide• Par Sterile Products LLC

Febuxostat 40mg (Sun Pharma) – microbial contamination (2024)

CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment.

Class IIModerate

FDAMar 4, 2024Nationwide• SUN PHARMACEUTICAL INDUSTRIES INC

Bread Butter White Bread (Albertsons) – Metal Contamination (2024)

Foreign object; metal and plastic shavings.

Class IIModerate

FDAMar 4, 2024CA, NV• Albertsons Companies LLC

ARCHITECT Anti-HCV Reagent Kit (Abbott) – False Elevated Results (2024)

Low

FDAMar 4, 2024Nationwide• Abbott GmbH Max-Planck-Ring 2 Wiesbaden Germany

Liquid Protein Calibrators (Randox) – Calibration Realignment (2024)

The firm has realigned C3 and Haptoglobin in Liquid Protein Calibrators, IT2691, to reference material ERM-DA470k/IFCC.

Low

FDAMar 1, 2024CA, FL, IL +4 more• Randox Laboratories Ltd. 55 Diamond Road Crumlin (North) Ireland

Entuit Suture Anchor Set (Cook) – Packaging Seal Strength Issue (2024)

Packaging may have low seal strength and not meet peel strength specifications, compromising device sterility

Moderate

FDAMar 1, 2024Nationwide• Cook Incorporated

Peel-Away Introducer (Cook) – Packaging Seal Strength Issue (2024)

Packaging may have low seal strength and not meet peel strength specifications, compromising device sterility

Moderate

FDAMar 1, 2024Nationwide• Cook Incorporated

Dilator Coons Taper (Cook) – Packaging Seal Strength Issue (2024)

Packaging may have low seal strength and not meet peel strength specifications, compromising device sterility

Moderate

FDAMar 1, 2024Nationwide• Cook Incorporated

Dilator (Cook) – Packaging Seal Strength Issue (2024)

Packaging may have low seal strength and not meet peel strength specifications, compromising device sterility

Moderate

FDAMar 1, 2024Nationwide• Cook Incorporated

Trocar Needle (Cook) – Packaging Seal Strength Issue (2024)

Packaging may have low seal strength and not meet peel strength specifications, compromising device sterility

Moderate

FDAMar 1, 2024Nationwide• Cook Incorporated

Medline Medical Procedure Kits (Medline) – Needle Guide Ring Detachment (2024)

Trumpet Needle Guide ring can detach when excessive pressure is applied.

Moderate

FDAMar 1, 2024Nationwide• MEDLINE INDUSTRIES, LP Northfield

Centurion OB Instrument Tray (Medline) – Needle Guide Ring Detachment (2024)

Trumpet Needle Guide ring can detach when excessive pressure is applied.

Moderate

FDAMar 1, 2024Nationwide• MEDLINE INDUSTRIES, LP Northfield

HeNe Laser System (Pacific LaserTech) – Key Control Noncompliance (2024)

These laser products fail to comply with 21 CFR 1040.10(f)(4) Key control which requires, Each laser system classified as a Class IIIb or IV laser product shall incorporate a key-actuated master control. The key shall be removable and the laser shall not be operable when the key is removed. , because while the laser is switched on, the key can be removed from the key switch. The correction is replacement with a key switch that captures the key when in the on position.

High

FDAMar 1, 2024Nationwide• PACIFIC LASERTECH, LLC

Faraday Future FF-91 Alliance (Faraday Future) – Air Bag Software Error (2024)

Faraday Future Eco Sales. LLC (FF) is recalling certain 2023 Faraday Future FF 91 2.0 Alliance vehicles. A software error may prevent the air bag malfunction warning light from illuminating when a system fault is detected in the Airbag Control Unit (ACU).

High

NHTSAMar 1, 2024Nationwide• FARADAY FUTURE

Chiba Biopsy Needle (Cook) – Packaging Seal Strength Issue (2024)

Packaging may have low seal strength and not meet peel strength specifications, compromising device sterility

Moderate

FDAMar 1, 2024Nationwide• Cook Incorporated

Triangle Tip Electrosurgical Knives (Olympus) – Breakage Warning (2024)

Due to increase in complaints for the KD-640L and KD-645L Triangle Tip Electrosurgical Knives breaking off during use -issuing reminder to users to utilize the electrosurgical knife in accordance with the Instructions for Use, which details critical specifications regarding electrosurgical unit compatibility and output due to reports of serious injury

Moderate

FDAMar 1, 2024Nationwide• Olympus Corporation of the Americas