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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

896

Class I (Serious)

125

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 17592 recalls

ARCHITECT 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

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

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

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Moderate

FDAMar 1, 2024Nationwide• Olympus Corporation of the Americas

DxI 9000 Access Immunoassay Analyzer (Beckman Coulter) – Pneumatic Tubing Disconnect (2024)

Laceration Risk

The reason for the recall is the pneumatic tubing used in the analytical pick-and-place (PnP) assembly cable may fully or partially disconnect from the flex cable assembly fittings during normal operation. The DxI 9000 Access Immunoassay Analyzer may generate a System Event log message that indicates PnP errors. Any cancelled tests will have an associated SYS flag. The analyzer may enter the Red-system status because of this issue. The analyzer also may not eject RVs, where unbound conjugate could potentially splash up on the sidewall of the RV, not being properly washed away, resulting in an artificially higher signal (RLU). The analyzer may not detect this splashing and continue with normal operation, which can cause false low or high erroneous results. Consequently, the analyzer may cancel in-progress tests. These errors could potentially cause delay reporting patient test results and patient treatments. The degree of the potential health hazard is dependent on the analytes that are potentially delayed, especially those analytes that would be used in the acute setting when treatment decisions are immediate. In this particular recall the highest risk analyte is troponin. Health consequences could include permanent impairment or possibly death if medical treatment decisions are delayed due to a delay in obtaining patient results. The issue was identified by Beckman Coulter Inc. manufacturing staff at their location in Brea California on February 29, 2024, during in-process acceptance inspection activities.

Very High

FDAFeb 29, 2024Nationwide• Beckman Coulter, Inc.

Phenylephrine HCl (SSM Health) – sterility validation (2024)

Lack of Assurance of Sterility: Firm did not perform process validation.

Class IIModerate

FDAFeb 29, 2024MO• SSM Health Care St. Louis DBA SSM St. Clare Health Center

FentaNYL Citrate (SSM Health) – sterility validation (2024)

Lack of Assurance of Sterility: Firm did not perform process validation.

Class IIModerate

FDAFeb 29, 2024MO• SSM Health Care St. Louis DBA SSM St. Clare Health Center

Powerade Zero Mixed Berry (Coca-Cola) - metal object (2024)

The potential presence of a foreign metal object in the product, i.e. a stainless-steel ring.

Class IIModerate

FDAFeb 27, 2024FL, IN, SC• THE COCA-COLA COMPANY

Powerade Mountain Berry Blast (Coca-Cola) - metal object (2024)

The potential presence of a foreign metal object in the product, i.e. a stainless-steel ring.

Class IIModerate

FDAFeb 27, 2024FL, IN, SC• THE COCA-COLA COMPANY

Powerade Zero Fruit Punch (Coca-Cola) - metal object (2024)

The potential presence of a foreign metal object in the product, i.e. a stainless-steel ring.

Class IIModerate

FDAFeb 27, 2024FL, IN, SC• THE COCA-COLA COMPANY

NUCAMP CIRRUS 820 (NUCAMP) – Electrical System Issue (2024)

Fire/Burn Risk

Pleasant Valley Teardrop Trailers LLC (Pleasant Valley) is recalling certain 2023-2024 nuCamp TAB 400, Cirrus 620, and 820 trailers with the Lithium Upgrade. The incorrect battery disconnect switch may have been installed.

High

NHTSAFeb 26, 2024Nationwide• NUCAMP

Altair Patient Lift (Human Care) – Hanger Bar Risk (2024)

Patient lift hanger bar may come loose, which could potentially pose risks to patients.

High

FDAFeb 23, 2024Nationwide• Human Care Hc Sweden Ab Arstaangsvagen 21 B Stockholm Sweden

RayStation Software (RaySearch) – Material Override Error (2024)

A use error that has occurred with RayStation/RayPlan, where material override using Silicon, Si, was incorrectly selected for a silicone gel polymer implant.

High

FDAFeb 23, 2024Nationwide• RAYSEARCH LABORATORIES AB Eugeniavagen 18c Stockholm Sweden

MATRYX Snowmobiles (Polaris) – Injury Risk (2024)

This recall involves certain Polaris Model Year 2022-2024 MATRYX Voyageur, Indy, Switchback, RMK, and SKS snowmobiles. The recalled snowmobiles were sold in black and custom color combinations and equipped with PATRIOT 650 and 850 engines. The recall also includes primary (drive) clutches sold as service parts with part numbers 1323613 (e-start) and 1323614 (manual start). "POLARIS" is stamped on the front side panel of the vehicles. The VIN and model number are located on the right side of the vehicle's frame. The following models are being recalled: Recalled Model Description Recalled Snowmobiles Model Description Model Year 2022 650 MATRYX VOYAGEUR 146 Model Year 2022 650 MATRYX INDY Model Year 2022 850 MATRYX INDY Model Year 2022 650 MATRYX SWITCHBACK Model Year 2022 850 MATRYX SWITCHBACK Model Year 2022 650 MATRYX RMK Model Year 2022 850 MATRYX RMK Model Year 2023 650 MATRYX INDY Model Year 2023 850 MATRYX INDY Model Year 2023 650 MATRYX SWITCHBACK Model Year 2023 850 MATRYX SWITCHBACK Model Year 2023 650 MATRYX VOYAGEUR 146 Model Year 2023 650 MATRYX SKS 146 Model Year 2023 650 MATRYX RMK Model Year 2023 850 MATRYX RMK Model Year 2024 850 MATRYX RMK

High

CPSCFeb 22, 2024Nationwide• Polaris Industries Inc., of Medina, Minnesota

Organic Carrot Juice (Barsotti) – Under Processed (2024)

Product was determined to be under processed.

Class IIModerate

FDAFeb 22, 2024AZ, CA, CT +7 more• Barsotti Juice Company, Inc.