Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K854816 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Integra® Long Epidural Steroid Injection Needle (Tuohy Needle), 20 gauge x 5 inch. Plastic Hub, Meta... | 2 | 07/09/2015 | Integra LifeSciences Corp. d.b.a. Integra Pain Management |
| Integra Long Epidural Steroid Injection Needle (Tuohy Needle), 18 Gauge x 5 inch Removable Wing, Met... | 2 | 04/29/2015 | Integra LifeSciences Corp. d.b.a. Integra Pain Management |
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