Product Recalls in Delaware
Product recalls affecting Delaware — including food, drugs, consumer products, medical devices, and vehicles distributed to Delaware. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,577 recalls have been distributed to Delaware in the last 12 months.
Showing 16441–16460 of 27,373 recalls
Recalled Item: Respire Pink+ Hard/Soft Oral Sleep Apnea Device Recalled by Respire Medical...
The Issue: Potential for device breakage during use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AERO IOL Injection System containing 10 Z28 Cartridges per box Recalled by...
The Issue: The recommended storage temperature on the label is incorrect.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elekta ERGO++ Product Usage: ERGO is often used for stereotactic treatments....
The Issue: Incorrect DICOM mapping of the exported collimator or couch angles from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Amia Automated Peritoneal Dialysis Set with Cassette Recalled by...
The Issue: The firm received increased customer complaints for Missing Red Line,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Respire Pink+ Hard Oral Sleep Apnea Device Recalled by Respire Medical Due...
The Issue: Potential for device breakage during use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mobile Mini C-arm system Part # 1000-0004. Intended to provide Recalled by...
The Issue: OrthoScan Inc. discovered during investigation of a non-standard work flow a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1113 Gravity Tube Set Pk/24 -SH Product Usage: The FMS Recalled by DePuy...
The Issue: Leakage of FMS gravity tub sets (281113) at the bulb and tube connection
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.via systems with SW VB20A Recalled by Siemens Medical Solutions USA,...
The Issue: A software update was released on August 22, 2017. Performing this software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mobile Mini C-arm system Part # 1000-0005. Intended to provide Recalled by...
The Issue: OrthoScan Inc. discovered during investigation of a non-standard work flow a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mobile Mini C-arm system Part # 1000-0001. Intended to provide Recalled by...
The Issue: OrthoScan Inc. discovered during investigation of a non-standard work flow a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mobile Mini C-arm system Part # 1000-0004-FD. Intended to provide Recalled...
The Issue: OrthoScan Inc. discovered during investigation of a non-standard work flow a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carl Zeiss INTRABEAM PRS 500 Recalled by Carl Zeiss Meditec AG Due to The...
The Issue: The device had an incorrect printed calibration value on the calibration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer¿ K2 EDTA (K2E) 3.6mg Blood Collection Tube (13 Recalled by...
The Issue: A limited portion of the lot was manufactured with less than the required...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Unify Recalled by St Jude Medical Inc. Due to The device may exhibit...
The Issue: The device may exhibit premature battery depletion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona Partial Knee System Product Usage: The Persona Partial Knee Recalled...
The Issue: Potential for the Persona Partial Knee Impactor Pad to fracture.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fortify VR - Model Numbers: CD1231-40 and CD1231-40Q Recalled by St Jude...
The Issue: The device may exhibit premature battery depletion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G7 DUAL MOBILITY LINER 44MM F Product Usage: Intended for Recalled by Zimmer...
The Issue: The affected products are labeled and etched as F-44 mm liners; however, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AGC 2000 LP Patella Recalled by Zimmer Biomet, Inc. Due to The affected AGC...
The Issue: The affected AGC 2000 LP Patella products were over-molded leaving the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AGC 2000 LP Patella Recalled by Zimmer Biomet, Inc. Due to The affected AGC...
The Issue: The affected AGC 2000 LP Patella products were over-molded leaving the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AArtis Q/ Q.Zen biplane Artis zee biplane Product Usage: Artis Recalled by...
The Issue: Within a specific number of Artis zee biplane and Artis Q biplane systems, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.