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Siemens Healthcare Diagnostics, Inc.

Siemens Healthcare Diagnostics, Inc. Recalls

All product recalls associated with Siemens Healthcare Diagnostics, Inc..

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Recall Summary

Total Recalls

1000

Past Year

593

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 1161–1180 of 10391 recalls

Atellica IM EPO Assay (Siemens) – Result Bias (2024)

Siemens Healthcare Diagnostics has confirmed an average negative bias of -35% compared to the 3rd World Health Organization (WHO) International Standard (NIBSC code: 11/170) that is proportional across the assay measuring interval. The reference interval as claimed in the Instructions for Use (IFU) is not achieved with affected lots.

FDAJan 24, 2024Nationwide• Siemens Healthcare Diagnostics, Inc.

Impression Coping (Thommen) – Canal Depth Issue (2024)

The depth of the internal canal was not manufactured according to specifications. Thus, the impression coping cannot be firmly connected to the implant.

FDAJan 24, 2024Nationwide• Thommen Medical AG Eschenweg 3 Bettlach Switzerland

Norepinephrine Injection (Baxter) – Label Concentration Error (2024)

Incorrect product concentration on the overwrap label: The overwrap label incorrectly identified the product strength as 4 mg / 250 mL; however, the primary bag label correctly identified the product strength as 8 mg / 250 mL.

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Class IIModerate

FDAJan 23, 2024Nationwide• Baxter Healthcare Corporation

Cotton Mattress Pads (Bokser Home) – Fire Hazard (2024)

Fire/Burn Risk

This recall involves all sizes of Bokser Home 100% cotton mattress pads manufactured after October 2022. The quilted box stitch pattern mattress pads have a 100% cotton shell and fill. The retailer's name, manufacturer, and date of manufacture are printed on a label on the mattress pad.

CPSCJan 18, 2024Nationwide• Anhui Zhongqinghonyu Home Textile Technology Co. LTD, of China

Adrenalin Epinephrine Injection (Henry Schein) – Incorrect Labeling (2024)

Labeling: Incorrect or Missing Lot and/or Exp Date. The expiration date listed on the Repack Pouch Label is incorrect.

Class IIModerate

FDAJan 17, 2024Nationwide• Henry Schein Inc. and Glove Club HSI Gloves Inc.

W&H Surgical Handpiece (W&H) – Laser Marking Error (2024)

1:2 speed increasing surgical handpieces have been incorrectly laser marked during production. The specific laser marking should read 1:2, but instead it reads 1:1 on the body of the handpiece

FDAJan 16, 2024Nationwide• W & H DENTALWERK BUERMOOS GMBH Ignaz Glaser Strase 53 53 IGNAZ-GLASER-STRASSE BUERMOOS Austria

Directional Laser Probe (D.O.R.C.) – Fiber Extension Problem (2024)

When using those products you may experience difficulties to extend or retract the laser fiber, and in some occasions may also have difficulties to direct the laser fiber tip precisely.

FDAJan 15, 2024Nationwide• D.O.R.C. Dutch Opthalmic Research Center Intl B.V. Scheijdelveweg 2 Zuidland Netherlands

Notoginseng Gout Granule (8th Ave Pharmacy) – Undeclared Drugs (2024)

Undeclared Allergen

Product contains undeclared Diclofenac and Dexamethasone Acetate

Class IIModerate

FDAJan 14, 2024AL, CO, FL +22 more• 8TH AVE PHARMACY

3M Specialty Blade Assembly (3M) – Burn Risk (2024)

Fire/Burn Risk

3M has added the following cautionary statement regarding the use of the product: "Caution - To reduce the risk of burns, which if not avoided may result in minor injury: " Do not use on injured skin. " Do not leave clipper running unused in air without applying to skin for more than 1 minute as blade temperature may exceed 41C (105.8F). " Do not leave the clipper blade applied to the same location on the patient s skin for longer than 1 second as potential injury may occur; continuous motion of the clipper during use is required. Note: If clipper is left running unused in air for 10 minutes without applying to skin, the Model 9690 blade maximum temperature may reach 60C (140F) and the Model 9660 blade maximum temperature may reach 77C (170.6F)."

FDAJan 12, 2024Nationwide• 3M Company Health Care Business 3m Center

Evaporator Coil Drain Pans (Daikin) – incorrect marking (2024)

Fire/Burn Risk

This recall expansion includes certain units manufactured between January 2019 and February 2020 that were incorrectly marked. DCT recently discovered that a limited number of evaporator coils that were manufactured during that time frame were incorrectly marked with a 2018 serial number, indicating that the unit was manufactured in 2018. The recall scope now includes about 3,600 additional units with the following configurations and coil serial numbers, as shown in the table below: Type Coil Configuration Affected Furnace Brands Affected Coil Serial Numbers Dates Sold Condensing furnace system Up-Flow (Coil above Furnace) All Prefixes ranging from 1901 through 2101 and certain prefixes ranging from 1811-1812 Jan. 2019 through Nov. 2021 Non-condensing furnace system (Certain configurations) Up-Flow (Coil above Furnace) Any "competitor" brand (excludes Goodman, Daikin or Amana branded furnaces) Prefixes ranging from 1901 through 2101 and certain prefixes ranging from 1811-1812 Jan. 2019 through Nov. 2021. NOTE: Furnace systems that were repaired with a new evaporator coil drain pan between January 2019 and November 2021, with the serial number range listed above, are also included in this recall. Whether a non-condensing furnace system falls within the scope of the recall depends on the location of the burners, which, if unknown, can be verified through DCT's model verification tool at: https://www.recallrtr.com/drainpan. Affected units can be identified through serial numbers found on the evaporator coil or the case, which sits atop the vertically installed furnace. The furnace brand and model number can be found on the furnace on the "Energy Guide" label. Consumers can refer to the instructions on Goodman's model verification tool at: https://www.recallrtr.com/drainpan. The model number of the outdoor condenser may also be required and can be found on a label attached to the product.

CPSCJan 11, 2024Nationwide• Daikin Comfort Technologies Manufacturing L.P. (f/k/a Goodman Manufacturing Company L.P.) of Houston, Texas

Rifampin Capsules (Amerisource) – Failed Impurities (2024)

Failed Impurities/Degradation Specification.

Class IIModerate

FDAJan 11, 2024Nationwide• Amerisource Health Services LLC