Medical Device Recalls
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71 to 80 of 500 Results
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Embrace Drill Tower, Standard/Lateral (25mm); Item Number: 645-081/63; | 2 | 03/27/2026 |
FEI # 3003386935 Waldemar Link GmbH & Co. KG (Mfg Site) |
| BD Kiestra" ReadA; Catalog No.: 446948. | 2 | 03/27/2026 |
FEI # 3010141591 BD KIESTRA LAB AUTOMATION |
| Sterile Radiology Procedure Kits, Model Number DYNDH1491B | 2 | 03/27/2026 |
FEI # 1417592 Medline Industries, LP |
| Puracol and Puracol Plus Collagen Wound Dressings: MSC8522 DRESSING,COLLAGEN,PURACOL,STRL,2" X 2"... | 2 | 03/27/2026 |
FEI # 1417592 Medline Industries, LP |
| Atellica CH Enzymatic Hemoglobin A1c (A1c_E); Siemens Material Number (SMN): 11097536; | 2 | 03/27/2026 |
FEI # 2432235 Siemens Healthcare Diagnostics, Inc. |
| ENFIT G-TUBE CONNECTOR, MEDLINE Item No. ENFIT1010GC | 2 | 03/27/2026 |
FEI # 1417592 Medline Industries, LP |
| Medline Kits containing ENFIT G-TUBE CONNECTOR 1. SKU DYKM2720 G/J TUBE CARE KIT 2. SKU ENFIT... | 2 | 03/27/2026 |
FEI # 1417592 Medline Industries, LP |
| Vue Motion V12. Product Number: 1017979. | 2 | 03/27/2026 |
FEI # 3002807880 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
| Allura Xper FD20/20; System Code: 722038; | 2 | 03/27/2026 |
FEI # 3042175844 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
| Azurion 5 M20; System Code: (1)722228, (2)722232, (3) 722281 (OUS only); | 2 | 03/27/2026 |
FEI # 3042175844 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
| * The maximium 500 devices meeting your search criteria returned. Please narrow your search. |
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