Medical DeviceJun 1, 2016
American Surgical Ray-Cot 1/2" x 2" Ref Number: 60-29 Product Usage: Neurosurgical and recall — FDA Z-1774-2016
Product packaging defective compromising sterility
Class IIFDA: TerminatedAmerican Surgical Company
28,992medical device recall records
2,381FDA Class I records
8firms with 5+ records
Zimmer Biomet, Inc.784 records
Database records
Records — page 1075
28,992 detailed records are currently available in this category.
Medical DeviceJun 1, 2016
American Surgical Cotton Balls-Strung 1/4" Ref Number: 30-00 Product Usage: Neurosurgical recall — FDA Z-1753-2016
Product packaging defective compromising sterility
Class IIFDA: TerminatedAmerican Surgical Company
Medical DeviceJun 1, 2016
American Surgical Telfa 1/2" x 3" Ref Number: 80-09 Product Usage: Neurosurgical and recall — FDA Z-1803-2016
Product packaging defective compromising sterility
Class IIFDA: TerminatedAmerican Surgical Company
Medical DeviceJun 1, 2016
American Surgical Telfa 1/2" x 1.5" Ref Number: 80-08 Product Usage: Neurosurgical and recall — FDA Z-1802-2016
Product packaging defective compromising sterility
Class IIFDA: TerminatedAmerican Surgical Company
Medical DeviceJun 1, 2016
American Surgical Delicot 30mm x 70mm Ref: 63-10 Product Usage: Neurosurgical and recall — FDA Z-1722-2016
Product packaging defective compromising sterility
Class IIFDA: TerminatedAmerican Surgical Company
Medical DeviceJun 1, 2016
American Surgical Ray-Cot 3" x 3" Ref Number: 60-15 Product Usage: Neurosurgical and recall — FDA Z-1772-2016
Product packaging defective compromising sterility
Class IIFDA: TerminatedAmerican Surgical Company
Medical DeviceJun 1, 2016
American Surgical Ray-Cot 1/2" x 1.5" Ref Number: 60-08 Product Usage: Neurosurgical and recall — FDA Z-1768-2016
Product packaging defective compromising sterility
Class IIFDA: TerminatedAmerican Surgical Company
Medical DeviceJun 1, 2016
American Surgical Delicot non-xray 5 mm x 8 mm Ref Number: 63-01 Non X-Ray Product Usage recall — FDA Z-1776-2016
Product packaging defective compromising sterility
Class IIFDA: TerminatedAmerican Surgical Company
Medical DeviceJun 1, 2016
American Surgical Ray-Cot 1/4" x 3" Ref Number: 60-04 Product Usage: Neurosurgical and recall — FDA Z-1765-2016
Product packaging defective compromising sterility
Class IIFDA: TerminatedAmerican Surgical Company
Medical DeviceJun 1, 2016
Draeger D-Vapor/ D-Vapor 3000 Vaporizers with Baxter Desflurane Agent and Bottles recall — FDA Z-1812-2016
Operators noticed unwanted release of evaporating anesthetic agent at the end of the filling procedure. Eye contact with volatile anesthetics can result in serious irritation. Immediate eye…
Class IIFDA: TerminatedDraeger Medical, Inc.
Medical DeviceJun 1, 2016
Synthes (USA) Products 3.2 mm three-fluted Radiolucent Drill Bit/Needle Point/145 mm Sterile recall — FDA Z-1710-2016
The sterile packaging may be compromised. A protective cap is to be secured on the tip of the drill bit. If the protective cap is not secured, the drill bit may puncture the sterile barrier.
Class IIFDA: TerminatedSynthes (USA) Products LLC
Medical DeviceJun 1, 2016
Ortho-Clinical Diagnostics 1) VITROS Immunodiagnostic Products Total Beta-hCG II Reagent recall — FDA Z-1700-2016
When testing was conducted using certain lots, VITROS Systems generated results within the measuring range for samples known to not contain measurable hCG. The system reported results up to…
Class IIFDA: TerminatedOrtho-Clinical Diagnostics
Medical DeviceJun 1, 2016
GE Medical Systems GE Healthcare, Discovery IGS 740 recall — FDA Z-1707-2016
Potential non-recoverable loss of image acquisition. The affected Discovery systems may experience multiple X-Ray abort errors before or during a real-time fluoroscopic Interventional…
Class IIFDA: TerminatedGE Medical Systems, LLC
Medical DeviceJun 1, 2016
American Surgical Ultracot 5 mm x 8 mm (Glassine) Ref Number: 23-01G Product Usage recall — FDA Z-1737-2016
Product packaging defective compromising sterility
Class IIFDA: TerminatedAmerican Surgical Company
Medical DeviceJun 1, 2016
American Surgical Delicot-J 15 mm x 20 mm Ref Number: 63-04J (Japan Only) Product Usage recall — FDA Z-1783-2016
Product packaging defective compromising sterility
Class IIFDA: TerminatedAmerican Surgical Company
Medical DeviceJun 1, 2016
American Surgical Policot 1/2" x 1.5" Ref Number: 90-08 Product Usage: Neurosurgical and recall — FDA Z-1809-2016
Product packaging defective compromising sterility
Class IIFDA: TerminatedAmerican Surgical Company
Medical DeviceJun 1, 2016
American Surgical Ultracot 5 mm x 8 mm Ref Number: 23-01 Product Usage: Neurosurgical and recall — FDA Z-1736-2016
Product packaging defective compromising sterility
Class IIFDA: TerminatedAmerican Surgical Company
Medical DeviceJun 1, 2016
American Surgical Americot Blue 3/8" x 3/4" Ref Number: 20-14S Product Usage: Neurosurgical recall — FDA Z-1729-2016
Product packaging defective compromising sterility
Class IIFDA: TerminatedAmerican Surgical Company
Medical DeviceJun 1, 2016
American Surgical Ultracot 13 mm x 60 mm Ref Number: 23-08 Product Usage: Neurosurgical and recall — FDA Z-1744-2016
Product packaging defective compromising sterility
Class IIFDA: TerminatedAmerican Surgical Company
Medical DeviceJun 1, 2016
American Surgical Delicot 5 mm x 13 mm Ref Number: 63-02 Product Usage: Neurosurgical and recall — FDA Z-1778-2016
Product packaging defective compromising sterility
Class IIFDA: TerminatedAmerican Surgical Company
Medical DeviceJun 1, 2016
American Surgical Telfa 1" x 3" Ref Number: 80-13 Product Usage: Neurosurgical and recall — FDA Z-1806-2016
Product packaging defective compromising sterility
Class IIFDA: TerminatedAmerican Surgical Company
Medical DeviceJun 1, 2016
American Surgical Ultracot 9 mm x 50 mm (Glassine) Ref Number: 23-07G Product Usage recall — FDA Z-1743-2016
Product packaging defective compromising sterility
Class IIFDA: TerminatedAmerican Surgical Company
Medical DeviceJun 1, 2016
American Surgical Americot Blue 1/8" x 1/8" Ref Number: 20-19S Product Usage: Neurosurgical recall — FDA Z-1730-2016
Product packaging defective compromising sterility
Class IIFDA: TerminatedAmerican Surgical Company
Medical DeviceJun 1, 2016
American Surgical Ray-Cot 1" x 3" Ref Number: 60-13 Product Usage: Neurosurgical and recall — FDA Z-1771-2016
Product packaging defective compromising sterility
Class IIFDA: TerminatedAmerican Surgical Company
How to use this medical device recall index
Medical device recall records can change as the FDA receives additional information. Check the official record identifier and current FDA information before making health or product-use decisions.
Recall Lookup USA keeps the last complete source record available when an official data service is temporarily unavailable. When a source provides only a few fields, we show only those known facts rather than padding the page with generic text.
What the database can and cannot tell you
This database is designed for discovery and reference. It can help you locate a relevant recall record, identify the recalling firm or NHTSA campaign, compare dates and classifications, and follow the official source. It is not a substitute for a VIN-specific NHTSA check, a manufacturer notice, medical advice or instructions issued by the recalling company.