Medical Device Recalls

121 to 130 of 500 Results *
Recall Date to: 07%2F14%2F2014

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Product Description	Recall Class	FDA Recall Posting Date	Recalling Firm
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Route 92 Medical, Tenzing 7 Delivery Catheter, REF 1005, Rx Only, Sterile EO. Used for introduction ...	1	04/24/2024	ROUTE 92 MEDICAL INC
QUIDEL InflammaDry MMP-9 Test, REF: PRS-ID-20-U, 20 Tests	2	04/24/2024	Quidel Corporation
QUIDEL InflammaDry MMP-9 Test, REF: PRS-ID-20, 20 Tests	2	04/24/2024	Quidel Corporation
Palindrome Precision HSI Chronic Catheter Sport Pack 14.5 Fr/Ch (4.8mm) x 19 cm (Symmetrical Tip, ...	2	04/24/2024	Covidien LP
Palindrome Precision H Chronic Catheter Kit 14.5 Fr/Ch (4.8mm) x 23 cm (Symmetrical Tip, Heparin C...	2	04/24/2024	Covidien LP
Mariner RDX MIS Polyaxial Head, REF: MX1-001010, part of Mariner RDX MIS Alpha Instruments and Impla...	2	04/23/2024	SEASPINE ORTHOPEDICS CORPORATION
LightStrike Blackout Curtains, Part numbers; 610-00008, 610-00009, 610-00019, 610-00020, and 610-000...	2	04/23/2024	XENEX Disinfection Services Inc.
48" Lead Wires, Replacement Part Number: 1067724-4	2	04/23/2024	EBI, LLC
Biomet OrthoPak Non-invasive Bone Growth Stimulator System-Indicated for the treatment of an establ...	2	04/23/2024	EBI, LLC
Biomet SpinalPak Non-invasive Spine Fusion Stimulator System- Indicated for the treatment of an est...	2	04/23/2024	EBI, LLC

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