Browse Device Recalls
3,096 FDA medical device safety recalls.
FDA Medical Device Recall Enforcement Database
Browse 3,096 FDA medical device recall enforcement actions. Each entry includes the device description, reason for recall, classification (Class I through III based on severity), recalling firm, and distribution details. Use the filters below to search by year, classification, state, or keyword.
Medical Device Recalls
Browse 3,096 FDA device recalls.
| Date | Product | Reason | Class | Firm |
|---|---|---|---|---|
| Jun 15, 2017 | Vis-U-All High Temp 7.5"x13" Self Seal Pouch 200 pouches per box; 4 boxes per... | On June 15, 2017, STERIS identified that the purple ink located on the outside label of Vis-U-All... | Class II | Steris Corporation |
| Jun 15, 2017 | Vis-U-All High Temp 16"x16" Heat Seal Pouch 100 pouches per box; 5 boxes per ... | On June 15, 2017, STERIS identified that the purple ink located on the outside label of Vis-U-All... | Class II | Steris Corporation |
| Jun 15, 2017 | Vis-U-All High Temp 4.5"x11" Heat Seal Pouch 200 pouches per box; 5 boxes per... | On June 15, 2017, STERIS identified that the purple ink located on the outside label of Vis-U-All... | Class II | Steris Corporation |
| Jun 15, 2017 | Vis-U-All High Temp 10"x15" Heat Seal Pouch 100 pouches per box; 5 boxes per ... | On June 15, 2017, STERIS identified that the purple ink located on the outside label of Vis-U-All... | Class II | Steris Corporation |
| Jun 15, 2017 | Vis-U-All High Temp 4"x8" Heat Seal Pouch 200 pouches per box; 5 boxes per ca... | On June 15, 2017, STERIS identified that the purple ink located on the outside label of Vis-U-All... | Class II | Steris Corporation |
| Jun 7, 2017 | Glidesheath Slender Hydrophilic Coated Introducer Sheath, 6FR - 10CM (0.021),... | An incomplete seal at the chevron end of the primary packaging of the GLIDESHEATH SLENDER Introdu... | Class II | Terumo Medical Corp |
| Jun 7, 2017 | Glidesheath Slender Hydrophilic Coated Introducer Sheath, 7FR - 10CM (0.021),... | An incomplete seal at the chevron end of the primary packaging of the GLIDESHEATH SLENDER Introdu... | Class II | Terumo Medical Corp |
| Jun 7, 2017 | Glidesheath Slender Hydrophilic Coated Introducer Sheath, 5FR - 10CM (0.021),... | An incomplete seal at the chevron end of the primary packaging of the GLIDESHEATH SLENDER Introdu... | Class II | Terumo Medical Corp |
| Jun 7, 2017 | Glidesheath Slender Hydrophilic Coated Introducer Sheath, 6FR - 16CM (0.021),... | An incomplete seal at the chevron end of the primary packaging of the GLIDESHEATH SLENDER Introdu... | Class II | Terumo Medical Corp |
| Jun 7, 2017 | Glidesheath Slender Hydrophilic Coated Introducer Sheath, 5FR - 16CM (0.021),... | An incomplete seal at the chevron end of the primary packaging of the GLIDESHEATH SLENDER Introdu... | Class II | Terumo Medical Corp |
| Jun 7, 2017 | Glidesheath Slender Hydrophilic Coated Introducer Sheath A-Kit, 6FR - 10CM (0... | An incomplete seal at the chevron end of the primary packaging of the GLIDESHEATH SLENDER Introdu... | Class II | Terumo Medical Corp |
| Jun 7, 2017 | Glidesheath Slender Hydrophilic Coated Introducer Sheath, 5FR - 10CM (0.021),... | An incomplete seal at the chevron end of the primary packaging of the GLIDESHEATH SLENDER Introdu... | Class II | Terumo Medical Corp |
| Jun 7, 2017 | DeRoyal(R) Dolphin Inflation Device, REF 0185ND, Rx Only, STERILE EO, Dolp... | Lack of sterility assurance. There is a defect in the primary packaging of the device, which may... | Class II | DeRoyal Industries Inc |
| Jun 7, 2017 | Glidesheath Slender Hydrophilic Coated Introducer Sheath A-Kit, 5FR - 16CM (0... | An incomplete seal at the chevron end of the primary packaging of the GLIDESHEATH SLENDER Introdu... | Class II | Terumo Medical Corp |
| Jun 7, 2017 | Glidesheath Slender Hydrophilic Coated Introducer Sheath A-Kit, 5FR - 10CM (0... | An incomplete seal at the chevron end of the primary packaging of the GLIDESHEATH SLENDER Introdu... | Class II | Terumo Medical Corp |
| Jun 7, 2017 | Glidesheath Slender Hydrophilic Coated Introducer Sheath A-Kit, 6FR - 16CM (0... | An incomplete seal at the chevron end of the primary packaging of the GLIDESHEATH SLENDER Introdu... | Class II | Terumo Medical Corp |
| Jun 7, 2017 | Glidesheath Slender Hydrophilic Coated Introducer Sheath, 5FR - 10CM (0.025),... | An incomplete seal at the chevron end of the primary packaging of the GLIDESHEATH SLENDER Introdu... | Class II | Terumo Medical Corp |
| Jun 7, 2017 | Glidesheath Slender Hydrophilic Coated Introducer Sheath, 7FR - 10CM (0.021),... | An incomplete seal at the chevron end of the primary packaging of the GLIDESHEATH SLENDER Introdu... | Class II | Terumo Medical Corp |
| Jun 7, 2017 | Glidesheath Slender Hydrophilic Coated Introducer Sheath, 6FR - 10CM (0.025),... | An incomplete seal at the chevron end of the primary packaging of the GLIDESHEATH SLENDER Introdu... | Class II | Terumo Medical Corp |
| Jun 7, 2017 | Glidesheath Slender Hydrophilic Coated Introducer Sheath A-Kit, 6FR - 10CM (0... | An incomplete seal at the chevron end of the primary packaging of the GLIDESHEATH SLENDER Introdu... | Class II | Terumo Medical Corp |
| Jun 7, 2017 | Glidesheath Slender Hydrophilic Coated Introducer Sheath A-Kit, 5FR - 10CM (0... | An incomplete seal at the chevron end of the primary packaging of the GLIDESHEATH SLENDER Introdu... | Class II | Terumo Medical Corp |
| Jun 7, 2017 | Glidesheath Slender Hydrophilic Coated Introducer Sheath, 6FR - 10CM (0.021),... | An incomplete seal at the chevron end of the primary packaging of the GLIDESHEATH SLENDER Introdu... | Class II | Terumo Medical Corp |
| Jun 7, 2017 | Glidesheath Slender Hydrophilic Coated Introducer Sheath, 7FR - 16CM (0.021),... | An incomplete seal at the chevron end of the primary packaging of the GLIDESHEATH SLENDER Introdu... | Class II | Terumo Medical Corp |
| May 22, 2017 | TUMARK Q, Length 12 cm, Diameter 18G, GTIN 04250195603081, REF 271500, STERILE | There is a potential risk of puncture to the packaging material which can compromise the devices ... | Class II | Somatex Medical Technologies GmbH |
| May 22, 2017 | Boston Scientific Zurpaz(TM) MEDIUM CURL, ASYMMETRIC CURVE, Steerable Sheath,... | Lack of sterility assurance. | Class II | Creganna Medical Devices |
| May 22, 2017 | Boston Scientific Zurpaz(TM) MEDIUM CURL, SYMMETRIC CURVE, Steerable Sheath, ... | Lack of sterility assurance. | Class II | Creganna Medical Devices |
| May 22, 2017 | Boston Scientific Zurpaz(TM) MEDIUM CURL, ASYMMETRIC CURVE, Steerable Sheath,... | Lack of sterility assurance. | Class II | Creganna Medical Devices |
| May 22, 2017 | Boston Scientific Zurpaz(TM) MEDIUM CURL, ASYMMETRIC CURVE, Steerable Sheath,... | Lack of sterility assurance. | Class II | Creganna Medical Devices |
| May 17, 2017 | QuikClot TraumaPad, , sterile, soft, white, X-ray detectable hemostatic dres... | Packaging breach may compromise sterility | Class II | Z-Medica, LLC |
| May 9, 2017 | Arrow MAC Two-Lumen Central Venous Access Kit Introducer Catheter The Arrow... | Arrow International is recalling the affected product because the packaging may not be completely... | Class II | Arrow International Inc |
| May 9, 2017 | 1) ARROWg+ard Blue You-Blend Two-Lumen Hemodialysis Catheterization Kit for H... | Arrow International is recalling the affected product because the packaging may not be completely... | Class II | Arrow International Inc |
| May 9, 2017 | 1) ARROWg+ard Blue MAC Two-Lumen Central Venous Access Kit 2) ARROWg+ard Blu... | Arrow International is recalling the affected product because the packaging may not be completely... | Class II | Arrow International Inc |
| May 9, 2017 | Single-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) Catheter... | Arrow International is recalling the affected product because the packaging may not be completely... | Class II | Arrow International Inc |
| May 9, 2017 | Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+a... | Arrow International is recalling the affected product because the packaging may not be completely... | Class II | Arrow International Inc |
| May 9, 2017 | 1) Pressure Injectable Multi-Lumen Central Venous Catheterization Kit 2) Pre... | Arrow International is recalling the affected product because the packaging may not be completely... | Class II | Arrow International Inc |
| May 9, 2017 | 1) Pressure Injectable ARROW(R) PICC Kit with Chlorag+ard(R) Technology The ... | Arrow International is recalling the affected product because the packaging may not be completely... | Class II | Arrow International Inc |
| May 9, 2017 | Arterial Catheterization Kit, Arterial Line Kit with Sharps Safety Features... | Arrow International is recalling the affected product because the packaging may not be completely... | Class II | Arrow International Inc |
| May 9, 2017 | 1) Introducer Kit with Integral Hemostasis Valve/Side Port, Sharps Safety Fea... | Arrow International is recalling the affected product because the packaging may not be completely... | Class II | Arrow International Inc |
| Apr 21, 2017 | Jackson-Pratt Silicone Flat Drain, 7mm, Full Ducts. Sterile, Rx Only. For Si... | Product's seal possibly compromised, potentially compromising the sterility of the package conten... | Class II | Cardinal Health 200, LLC |
| Apr 21, 2017 | Jackson-Pratt Hemaduct Silicone Round Drain, 19FR W/15FR Trocar. Sterile, Rx ... | Product's seal possibly compromised, potentially compromising the sterility of the package conten... | Class II | Cardinal Health 200, LLC |
| Apr 21, 2017 | Jackson-Pratt Silicone Flat Drain, 10mm, 3/4 Ducts. Sterile, Rx Only. For Si... | Product's seal possibly compromised, potentially compromising the sterility of the package conten... | Class II | Cardinal Health 200, LLC |
| Apr 21, 2017 | Jackson-Pratt Silicone Flat Drain, 10mm Full W/Trocar. Sterile, Rx Only. For... | Product's seal possibly compromised, potentially compromising the sterility of the package conten... | Class II | Cardinal Health 200, LLC |
| Apr 21, 2017 | Jackson-Pratt Hemaduct Silicone Round Drain, 10FR W/Trocar. Sterile, Rx Only.... | Product's seal possibly compromised, potentially compromising the sterility of the package conten... | Class II | Cardinal Health 200, LLC |
| Apr 21, 2017 | Jackson-Pratt Silicone Flat Drain, 7mm Full W/Trocar. Sterile, Rx Only. For ... | Product's seal possibly compromised, potentially compromising the sterility of the package conten... | Class II | Cardinal Health 200, LLC |
| Apr 21, 2017 | Jackson-Pratt Hemaduct Silicone Flat Drain, 10mm, Full Ducts W/15FR Trocar. ... | Product's seal possibly compromised, potentially compromising the sterility of the package conten... | Class II | Cardinal Health 200, LLC |
| Apr 21, 2017 | Jackson-Pratt Hemaduct Silicone Round Drain, 10FR W/10FR Trocar. Sterile, Rx ... | Product's seal possibly compromised, potentially compromising the sterility of the package conten... | Class II | Cardinal Health 200, LLC |
| Apr 21, 2017 | Jackson-Pratt Silicone Round Drain, 10FR. Sterile, Rx Only. For Single Use O... | Product's seal possibly compromised, potentially compromising the sterility of the package conten... | Class II | Cardinal Health 200, LLC |
| Apr 21, 2017 | Jackson-Pratt Hemaduct Silicone Round Drain, 15FR W/15FR Trocar. Sterile, Rx ... | Product's seal possibly compromised, potentially compromising the sterility of the package conten... | Class II | Cardinal Health 200, LLC |
| Apr 21, 2017 | Jackson-Pratt Hemaduct Silicone Round Drain, 10FR W/Trocar. Sterile, Rx Only.... | Product's seal possibly compromised, potentially compromising the sterility of the package conten... | Class II | Cardinal Health 200, LLC |
| Apr 21, 2017 | Jackson-Pratt Hemaduct Cardiothoracic Silicone Round Drain,19FR. Sterile, Rx... | Product's seal possibly compromised, potentially compromising the sterility of the package conten... | Class II | Cardinal Health 200, LLC |
Frequently Asked Questions
When a device safety issue is identified, the manufacturer or FDA initiates a recall. The FDA publishes an enforcement report detailing the device, the reason for the recall, and distribution. Healthcare facilities and providers are notified to check their inventory and take corrective action.
All types — from simple devices like blood glucose test strips and surgical gloves to complex devices like pacemakers, defibrillators, insulin pumps, hip implants, and ventilators. Software-driven devices are increasingly common in recalls due to bugs and cybersecurity vulnerabilities.
Use the search and filter tools on this page. Each recall entry includes the device description, model numbers, and distribution details so you can determine if your device is affected. Contact your healthcare provider if you find a match.