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Nichols Institute Diagnostics

Nichols Institute Diagnostics Recalls

All product recalls associated with Nichols Institute Diagnostics.

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Recall Summary

Total Recalls

1000

Past Year

1000

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 20601–20620 of 21319 recalls

Nichols Institute Diagnostics: Nichols Advantage 25-Hydroxy Vitamin D Assay, Catalog num...

Lower than expected results are obtained.

FDAJun 30, 2004Nationwide• Nichols Institute Diagnostics

Roche Diagnostics Corp.: ACCU-CHEK Inform meter; catalog No. 3035123.

Exposure to excessive disinfectant or cleaning solution may cause overheating, melting, or smoke.

FDAJun 30, 2004Nationwide• Roche Diagnostics Corp.

Roche Diagnostics Corp.: ACCU-CHEK Inform base unit; catalog no. 3035131.

Exposure to excessive disinfectant or cleaning solution may cause overheating, melting, or smoke.

FDAJun 30, 2004Nationwide• Roche Diagnostics Corp.

1...1029 103010311032 1033...1066

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Aaron Medical Industries, Inc.: Battery-operated Cautery High Temperature, fine/Loop/ Va...

The cover caps on some of these cauteries are not properly engaged to prevent inadvertent activation.

FDAJun 29, 2004IN• Aaron Medical Industries, Inc.

Aaron Medical Industries, Inc.: Battery-operated Cautery Low Temperature, fine/elongated...

The cover caps on some of these cauteries are not properly engaged to prevent inadvertent activation.

FDAJun 29, 2004IN• Aaron Medical Industries, Inc.

Smiths Medical ASD, Inc.: Portex Hypodermic Needle-Pro Syringe and Needle 1ml/LS Sm...

Sterility of product is not assured

FDAJun 29, 2004Nationwide• Smiths Medical ASD, Inc.

Gas-Powered Hand Tools (Echo) – Operational Safety (2004)

Fire/Burn Risk

The specific gas-powered tools involved are identified by the model and serial numbers on the following chart. The model number and serial number is written on the name plate on each product. Model Description Start S/N End S/N HC-150 Hedge Clipper 05036751 05076594 HC-150i Hedge Clipper 05003843 05005681 HC-151 Hedge Clipper 06005083 06007241 HCR-150 Hedge Clipper 05001362 05002577 HCR-151 Hedge Clipper 06001227 06001271 SHC-210 Hedge Clipper 05006409 05009843 SHC-211 Hedge Clipper 06001001 06001029 PB-200 Power Blower 05113414 05210165 PB-200 Power Blower 06015814 06028130 PE-200 Power Edger 05022289 05044753 PE-310 Power Edger 03001851 03003116 PE-311 Power Edger 02001085 02001266 PPF-210 Power Pruner 05009112 05014016 PPF-211 Power Pruner 06001278 06001423 ES-210 Shred/n/Vac 05037462 05061058 ES-211 Shred/n/Vac 06001999 06003588 GT-200i Trimmer 05020627 05030474 GT-200R Trimmer 05047380 05147265 GT-201i Trimmer 06001645 06001841 GT-201R Trimmer 06008111 06013438 SRM-210 Trimmer 05120420 05278091 SRM-210i Trimmer 05011856 05022111 SRM-210SB Trimmer 05008493 05016331 SRM-211 Trimmer 06009599 06016954 SRM-310 Trimmer 03005081 03008383 SRM-310S Trimmer 03001968 03003296 SRM-311 Trimmer 02003200 02003724 SRM-311S Trimmer 02001347 02001431 SRM-340 Trimmer 03001561 03002148 SRM-210U Brushcutter 05002961 05004671 SRM-211U Brushcutter 06001001 06001028 SRM-310U Brushcutter 03001782 03002571 SRM-311U Brushcutter 02001405 02001601 WP-1000 Water Pump 508419 510025

CPSCJun 29, 2004Nationwide• Echo Inc., of Lake Zurich, Ill.

Boston Scientific Corp: Boston Scientific brand Nephroureteral Stent System. Con...

Mislabeled as to size; 10FR are labeled as 8FR.

FDAJun 25, 2004MO• Boston Scientific Corp

ABX Diagnostics Inc: PENTRA 120 and PENTRA 120 Retic Hematology Analyzer

Power failure having impact on software.

FDAJun 24, 2004Nationwide• ABX Diagnostics Inc

Boston Scientific Corp: EMCEE OBTURATOR (7F) for use with 8F Sheath, REF #9258000...

Product labeled to contain Emcee Obturators contained Emcee Dilators.

FDAJun 24, 2004IN, NJ• Boston Scientific Corp

Varian Medical Systems Inc: medical device and software systems

a malfunction in the software of the VARiS versions 6.2.27 and 6.2.35 which is used to set up radiation therapy devices which will reset parameters to null for future treatments if a patient receives treatment on a non-varian machine and a varian machine and a non-varian field is loaded in the treatment session.

FDAJun 24, 2004Nationwide• Varian Medical Systems Inc

Argon Medical Devices, Inc: Argon Medical Devices, Vesseloops, Blue Maxi, Two Latex f...

Inadequate closure compromising sterility.

FDAJun 22, 2004CA, IN, MO +7 more• Argon Medical Devices, Inc

Basic Editions Girls' Rompers (Kmart) – Design Safety Issue (2004)

Choking Hazard

The recalled rompers are pink and white gingham with pink buttons and crocheted cherry-shape tassels on the pocket and green and white gingham bows on the trim of the leg openings. The rompers were sold in infant sizes 12 months to 24 months and toddler sizes 2T to 5T. "MADE IN/HECHO EN BANGLADESH" and "basic EDITIONS®" is printed on a label inside the neck of the garment.

CPSCJun 22, 2004Nationwide• Kmart Corporation, of Troy, Mich.

Toshiba American Med Sys Inc: Digital Radiography System, model DFP-8000D

Defect in the mirroring unit.

FDAJun 18, 2004Nationwide• Toshiba American Med Sys Inc

Advance Medical Designs Inc: Advance Medical''s, The Closed Camera System, 9'' x 96'' ...

The product may come apart when excessive force is applied to the coupler.

FDAJun 18, 2004Nationwide• Advance Medical Designs Inc

Roche Diagnostics Corp.: Roche/Hitachi brand ONLINE TDM Phenytoin; Contents of kit...

May report falsely decreased patient results.

FDAJun 18, 2004Nationwide• Roche Diagnostics Corp.

Boston Scientific Corp: Boston Scientific/Microvasive brand Biliary Stent Kit, 7 ...

Mislabeled as to length; 10 cm length labeled as 5 cm.

FDAJun 18, 2004CA, HI, KY +2 more• Boston Scientific Corp

Staar Surgical Co Inc: STAAR Surgical Intra Occular Lens, Collamer.

Mislabeled in part. Label set, patient chart labels, and patient ID card serial number did not match the IOL serial number.

FDAJun 17, 2004Nationwide• Staar Surgical Co Inc

Boston Scientific Corp: Boston Scientific/MEDI-TECH brand Fascial Dilator, 8 FR(2...

Labeling mix-up as to product size; 8FR may be labeled 10FR and vice versa.

FDAJun 16, 2004Nationwide• Boston Scientific Corp

Siemens Medical Solutions USA, Inc: ACOM.M angiographic x ray system. Model number 4371741

possible problem reviewing images on the ACOM.M

FDAJun 16, 2004AL, AZ, AR +32 more• Siemens Medical Solutions USA, Inc