Stay Informed

Get email alerts when new recalls match your interests.

Recall data is updated hourly from official government sources. Very recent recalls may not yet appear. About our data sources

About

We make U.S. recall data searchable and accessible for consumers and businesses.

Site

FAQ
Browse by State
Statistics
Recall Classifications
About
Enterprise API

Legal

Privacy Policy
Terms of Service
Report Incorrect Info

Official Sources

FDA Recalls ↗
USDA FSIS ↗
CPSC Recalls ↗
NHTSA Recalls ↗

RSS Feed

Home
/
Brands
/
Steris Corporation Hopkins Facility

Steris Corporation Hopkins Facility Recalls

All product recalls associated with Steris Corporation Hopkins Facility.

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

353

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 1021–1040 of 3680 recalls

Verify SixCess Challenge Pack (Steris) – Chemical Indicator Error (2022)

Product contains incorrect chemical indicators in packaging.

Low

FDAAug 10, 2022AK, AZ, AR +28 more• Steris Corporation Hopkins Facility

Neostigmine Injection (Nephron) – Manufacturing Contamination (2022)

CGMP Deviations: Potential for cross-contamination due to product carryover during manufacturing.

Class IIModerate

FDAAug 10, 2022Nationwide• Nephron Sterile Compounding Center LLC

Bupivacaine HCl Injection (Nephron) – Manufacturing Contamination (2022)

CGMP Deviations: Potential for cross-contamination due to product carryover during manufacturing.

Class IIModerate

1...50 515253 54...184

Page 52 of 184Next

FDAAug 10, 2022Nationwide• Nephron Sterile Compounding Center LLC

Trisodium Citrate Solution (Nephron) – Manufacturing Contamination (2022)

CGMP Deviations: Potential for cross-contamination due to product carryover during manufacturing.

Class IIModerate

FDAAug 10, 2022Nationwide• Nephron Sterile Compounding Center LLC

Labetalol HCl Injection (Nephron) – Manufacturing Contamination (2022)

CGMP Deviations: Potential for cross-contamination due to product carryover during manufacturing.

Class IIModerate

FDAAug 10, 2022Nationwide• Nephron Sterile Compounding Center LLC

CorVocet Biopsy System (Merit) – Needle Ejection (2022)

Biopsy Systems have components that are misaligned due to an issue with the manufacturing assembly equipment, which may lead to the needle ejecting when triggered outside the body, which may result in user or patient needle stick injury.

High

FDAAug 3, 2022AL, AK, AZ +40 more• Merit Medical Systems, Inc.

Underwater Communication Devices (Ocean Technology) – fire hazard (2022)

Fire/Burn Risk

This recall involves the PowerCom 3000D, 5000D and MilCom 6000D underwater communication devices sold with the RBLi-4 Lithium battery pack and the batteries that are also sold separately. The PowerCom, MilCom and RBLi-4 products are used in all SCUBA diving. The recalled RBLi-4 battery packs are in a waterproof housing and supply power to the PowerCom and MilCom products. PowerCom and MilCom along with the model numbers are printed on the front of the underwater communication devices.

High

CPSCJul 28, 2022Nationwide• Undersea Systems International Inc., dba Ocean Technology Systems, of Santa Ana, California

FentaNYL Citrate IV Bags (SterRx) – Sterility Issue (2022)

Lack of Assurance of Sterility

Class IIModerate

FDAJul 25, 2022Nationwide• SterRx, LLC

FentaNYL Citrate IV Bags (SterRx) – Sterility Concern (2022)

Lack of Assurance of Sterility

Class IIModerate

FDAJul 25, 2022Nationwide• SterRx, LLC

HLS Set Advanced (Maquet) – Sterility Barrier (2022)

The firm has expanded the recall for the HLS Set Advanced regarding a potential breach in the sterility barrier that may result in compromised product sterility (prior recall was initiated November 6, 2020).

Moderate

FDAJul 22, 2022Nationwide• Maquet Medical Systems USA

Corin MetaFix Hip Stem (Corin) – Incorrect Labeling (2022)

One MetaFix size 7 collarless stem from batch 478179 which was incorrectly labelled as a MetaFix size 3 collared stem from batch 485630.

Low

FDAJul 22, 2022Nationwide• Corin Ltd Unit 1-57-8 Corinium Centre Cirencester United Kingdom

Towmaster TC-14D Trailer (Towmaster) – Tire Load Rating (2022)

Monroe Towmaster, LLC (Monroe Towmaster) is recalling certain 2021-2022 TC-14D, T-24, and TC-24 trailers. The tire load rating on the installed tires is less than the capacity rating of the trailer. Tires installed onto trailers were "E" rated instead of the required "F" rating. As such, these vehicles fail to comply with the requirements of the Federal Motor Vehicle Safety Standard (FMVSS) number 109, "New Pneumatic and certain specialty tires," and number 119, "New Pneumatic Tires-Other Than Passenger Cars."

High

NHTSAJul 22, 2022Nationwide• TOWMASTER