| 2026-05-06 | NHTSA | Contact with Drive Belt Pully May Damage and Cause Oil Lines to Leak | Corp. Micro Bird, Inc. | N/A | 902 |
| 2026-05-06 | FDA Device | FDA Recall: Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: SPNG NEURO 1X1 | Medline Industries, LP | Class II | N/A |
| 2026-05-06 | FDA Device | FDA Recall: Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: 1. ANTERIOR | Medline Industries, LP | Class II | N/A |
| 2026-05-06 | FDA Device | FDA Recall: Brand Name: HiResolution" Bionic Ear System Product Name: M Zn-Air Battery Pak Model/Catalog Numbe | Advanced Bionics, LLC | Class II | N/A |
| 2026-05-06 | FDA Device | FDA Recall: Philips Ingenia Ambition X with MR Elastography (MRE). 1. Model Number (REF): 781356. 2. Mod | Philips North America | Class II | N/A |
| 2026-05-06 | FDA Device | FDA Recall: Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 4 CEM. Part Number: 150450204. | DEPUY (IRELAND) | Class II | N/A |
| 2026-05-06 | FDA Drug | FDA Recall: fentaNYL Citrate Injectable Solution, Narcotic, CII, 1250 mcg/25mL (50 mcg per mL), 25 mL, wells pha | Wells Pharma of Houston LLC | Class II | N/A |
| 2026-05-06 | FDA Drug | FDA Recall: fentaNYL Citrate Injectable Solution, NARCOTIC, Cii, 1000 mcg/100 mL (10 mcg per mL), 100 mL bag, We | Wells Pharma of Houston LLC | Class II | N/A |
| 2026-05-06 | FDA Drug | FDA Recall: GenTeal Tears, Lubricant Eye Gel, Sterile, 10g (0.34 Fl oz), Distributed by: Alcon Laboratories, Inc | Alcon Research LLC | Class II | N/A |
| 2026-05-06 | FDA Device | FDA Recall: WHILL Model F, with software versions before HMI: 2.23 / MC: 1.05; the device is an indoor/outdoor, | WHILL, INC. | Class I | N/A |
| 2026-05-06 | FDA Device | FDA Recall: WHILL Model C2, with software versions before HMI: 2.22 / MC: 1.13; device is an indoor/outdoor batt | WHILL, INC. | Class I | N/A |
| 2026-05-06 | FDA Device | FDA Recall: Brand Name: Genius" Review Station Product Name: Genius" Review Station Display (Barco Monitor) Mo | Hologic, Inc | Class II | N/A |
| 2026-05-06 | FDA Device | FDA Recall: Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: 1. CATARACT | Medline Industries, LP | Class II | N/A |
| 2026-05-06 | FDA Device | FDA Recall: Medline and Centurion medical procedure kits, containing Medline Neuro Sponges (1229 in total), HEAD | Medline Industries, LP | Class II | N/A |
| 2026-05-06 | FDA Device | FDA Recall: Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: 1. PLASTICS | Medline Industries, LP | Class II | N/A |
| 2026-05-06 | FDA Device | FDA Recall: Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: 1. SPINE PROCE | Medline Industries, LP | Class II | N/A |
| 2026-05-06 | FDA Device | FDA Recall: Philips SmartPath to dStream for 3.0T with MR Elastography (MRE). 1. Model Number (REF): 782145. | Philips North America | Class II | N/A |
| 2026-05-06 | FDA Drug | FDA Recall: Similasan, iVIZIA, Sterile Lubricant Eye Drops (Povidone 0.5%), 0.33 Fl oz (10 mL), Made in France, | Thea Pharma, Inc. | Class II | N/A |
| 2026-05-06 | FDA Food | FDA Recall: Black label with blue lettering. FOOD Korean Food, ENOKI MUSHROOM, 150g clear plastic package; Produ | HEMU TRADING INC | Class I | N/A |
| 2026-05-06 | FDA Device | FDA Recall: Philips Bridge Prep Kit REF: K12-09098B Sterile EO, Rx ONLY | Merit Medical Systems, Inc. | Class II | N/A |
| 2026-05-06 | FDA Food | FDA Recall: KLG, Kesar Mukhwas, perishable, 24 months, flexible plastic, 200 gm, 818812022208, Ganesha Enterpris | Ganesha Enterprises LLC | Class II | N/A |
| 2026-05-06 | FDA Device | FDA Recall: Medline medical procedure kits, containing Medline Neuro Sponges (4077 in total), LAMINECTOMY, CRANI | Medline Industries, LP | Class II | N/A |
| 2026-05-06 | FDA Drug | FDA Recall: Lidocaine Wound Gel (Benzalkonium Chloride, 0.13% and Lidocaine Hydrochloride, 2%), NET WT 0.5 OZ (1 | Water-Jel Technologies, LLC | Class III | N/A |
| 2026-05-06 | FDA Device | FDA Recall: Medtronic Sphere-9 Catheter, Model Number AFR-00001; catheter, percutaneous, cardiac ablation, for t | Medtronic, Inc. | Class II | N/A |
| 2026-05-06 | FDA Food | FDA Recall: 52USA brand POPPING BOBA; PASSION FRUIT FLAVOR; Net wt: 7 lb (3.2kg); Ingredients Drinking water, fr | Guangdong Zonegoing Food Co., LTD | Class II | N/A |