Recent federal regulations affecting small businesses
Page 153 of 158 • Last updated April 8, 2026
2365 new federal regulations affecting small businesses have been published in the past 30 days, drawn from the Federal Register, FDA recalls, and USDA notices. Each listing links straight to the official source so you can read the full text and respond if it touches your business.
- Intuitive Surgical, Inc.: Brand Name: da Vinci S, Si Mega Needle Driver Instrument Product Name: da Vinci S, Si Mega Needle Driver Instrument Model/Catalog Number: 420194 Software Version: NA P...April 8, 2026
Intuitive Surgical recalls 7,819 da Vinci S and Si Mega Needle Driver instruments worldwide due to broken or frayed grip cables that may cause temporary health problems.
- PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: ALLURA Xper FD20 Biplane; System Code: (1) 722008, (2)722013; and 21 other productsApril 8, 2026
Philips Medical Systems recalls 461 units (198 in US) of ALLURA Xper FD20 biplane X-ray systems due to wired foot switch malfunction that may prevent or intermittently disable imaging initiation.
- Synthes (USA) Products LLC: 2.4 VOLT TAP LOCKING SCREW TAP TO 90MM. Part Number: 03.424.124-US and 1 other productApril 8, 2026
Synthes USA Products recalls 77 units of 2.4 Volt Tap Locking Screw Tap (Class II) due to lot swap resulting in incorrect threading; distributed nationwide across 22 states.
- BD KIESTRA LAB AUTOMATION: BD Kiestra" ReadA; Catalog No.: 446948April 8, 2026
BD Kiestra ReadA lab automation system (Catalog No. 446948) issued Class II recall affecting 82 units for potential connectivity issues causing delays in plate retrieval after system reboot, with no impact on test results or sample integrity.
- Medline Industries, LP: THORACIC ROBOTS, DYNJ908777B and 6 other productsApril 8, 2026
Medline Industries recalls Class II thoracic robot kits containing defective Olympus biopsy valves that may shed rubber fragments into patients' airways, potentially requiring surgical removal.
- HEYTEA USA INC: Coconut Drink 1; NET VOLUME: 1L; Ingredients: Coconut water, freshly squeezed coconut gravy, white granulated sugar, emulsion stabilizer [sodium caseinate, mono- and diglycerides fa...April 8, 2026
HEYTEA USA Inc recalls 12,677 cartons of Coconut Drink 1 across seven states due to undeclared milk that may cause temporary health problems.
- TG FOODS INC: Divided Sunset Multi Collagen Peptides, 8 Ounce, Stand-up PouchApril 8, 2026
TG Foods Inc. recalls 7,980 units of Divided Sunset Multi Collagen Peptides nationwide due to missing allergen labeling for egg and fish species on the product.
- Super World Trading Inc.: MEI HEONG YUEN TANGERINE FLAVOR ROASTED PEANUTS; NET 9.17 oz (260g); Ingredients: Peanuts, Salt, Sugar, Liquorice, Spices, Sodium Cyclamate, Acesulfame-K, Vanilla, Ethyl M...April 8, 2026
Super World Trading Inc. recalls 595 cases of tangerine-flavored roasted peanuts distributed across 18 states due to banned cyclamate sweetener content.
- Oxoid Australia Pty Limited: OXOID MICROBACT IDENTIFICATION KITS, Listeria 12L Kit, 20 Tests; Listeria identification sysystemApril 8, 2026 • Impact: medium
Oxoid Australia's Microbact 12L identification kit (lot 4494873) is subject to a Class II recall due to potential misidentification of organisms from inconclusive color reactions; 2 kits distributed nationwide in Georgia and California.
- Abiomed, Inc.: Automated Impella Controller (AIC), labeled as the following with corresponding Product Codes: 1. Impella Controller, Packaged, CA; Product Code: 0042-0000-CA. 2. Impella Con...April 8, 2026
Abiomed recalls 62 Automated Impella Controller units internationally due to potential delay in "Purge System Blocked" alarm display with first generation Impella 5.5 pumps, classified as Class I.
- Olympus Corporation of the Americas: Brand Name: Olympus SOLTIVE Premium SuperPulsed Laser System Product Name: SOLTIVE Premium Laser System TFL-PLS Model/Catalog Number: TFL-PLS containing TFL-C...April 8, 2026
Olympus recalls 408 SOLTIVE Premium laser systems worldwide due to a defective 24V power supply module that may render units inoperable or produce smoke and burning smells within the enclosed console.
- PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: Vue Motion V12. Product Number: 1017979April 8, 2026
Philips Medical Systems recalls 3,552 Vue Motion V12 ultrasound systems (Product 1017979) worldwide due to potential frame sequencing errors during dynamic imaging that may cause temporary health complications.
- Siemens Healthcare Diagnostics, Inc.: Atellica CH Enzymatic Hemoglobin A1c (A1c_E); Siemens Material Number (SMN): 11097536;April 8, 2026
Siemens Healthcare Diagnostics Class II recall of Atellica CH Enzymatic Hemoglobin A1c test (SMN 11097536) due to potential depressed results when processing with RCRP on the same analyzer.
- Abiomed, Inc.: Purge Cassette, sold within Impella Pump Sets and Individually Packaged. Labeled and distributed in the below configurations and corresponding product codes. 1. Purge Cassette, 5 ...April 8, 2026
Abiomed recalls 33,107 Generation 1 purge cassettes distributed worldwide in Impella Pump Sets due to increased purge leak risk that may cause serious injury or death.
- ReCor Medical Inc.: Brand Name: Paradise¿ Ultrasound Renal Denervation System Product Name: Paradise ¿ Catheter Model/Catalog Number: PRDS-068-02 Product Description: Common name: Ablation cathe...April 8, 2026
ReCor Medical's Paradise ultrasound renal denervation catheter (Model PRDS-068-02) is subject to a Class II recall affecting 24 units distributed across nine U.S. states due to nonconforming product that should have been scrapped.