Product Recalls in California
Product recalls affecting California — including food, drugs, consumer products, medical devices, and vehicles distributed to California. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,940 recalls have been distributed to California in the last 12 months.
Showing 16961–16980 of 30,923 recalls
Recalled Item: XLTEK EMU40EX EEG Headbox Recalled by Natus Neurology DBA Excel Tech., Ltd....
The Issue: Possible degradation of an internal electronic component over time which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Draeger Jaundice Meter JM-103 The device is intended for use in hospitals...
The Issue: Users have misinterpreted the display for out of range measurement indicated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Draeger Jaundice Meter JM-105 The device is intended for use in hospitals...
The Issue: Users have misinterpreted the display for out of range measurement indicated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Minicon Clinical Sample Concentrators for In Vitro Diagnostic Use 9031...
The Issue: In vitro diagnostic devices, used greater than 6 months after date of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-Two Equinox¿ Relieve N2O/O2 Analgesic Gas Mixing and Delivery System...
The Issue: Higher levels of nitrous oxide delivered than specification
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AdvanDx QuickFISH Slides Recalled by Opgen Inc Due to Possible diminished...
The Issue: Possible diminished performance prior to its established expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safety Sideport Knife 1.0mm 45¿ Recalled by Beaver Visitec Due to Blades are...
The Issue: Blades are loose in handles and may fall out due to non cured epoxy
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus JF-140F duodenoscopes (Model NumberJF-140F) Recalled by Olympus...
The Issue: Issuance of validated, new reprocessing procedures. This corrective action...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus JF-160F duodenoscopes (Model NumberJF-160F) Recalled by Olympus...
The Issue: Issuance of validated, new reprocessing procedures. The new cleaning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard Knee System PS Tibial Bearing Recalled by Zimmer Biomet, Inc. Due...
The Issue: The label master file was errantly set up as a 63/37mm instead of a 63/67mm....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Outer Package Label: Tapered Screw-Vent Implant System Recalled by Zimmer...
The Issue: Dental implants have incorrect item/lot numbers and size on the inner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rio System Irrigation Clip - Catalog # 111690 Product Usage: Recalled by...
The Issue: Out of tolerance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GIBCO CTS AIM V Serum-Free Media (SFM) Recalled by Life Technologies, Corp....
The Issue: It has been determined that the fill port tube seal integrity was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gibco Dulbecco's Modified Eagle Medium (DMEM) Recalled by Life Technologies,...
The Issue: It has been determined that the fill port tube seal integrity was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gibco CTS OpTmizer T Cell Expansion Serum Free Medium Recalled by Life...
The Issue: It has been determined that the fill port tube seal integrity was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gibco Dulbecco's Modified Eagle Medium (DMEM) Recalled by Life Technologies,...
The Issue: It has been determined that the fill port tube seal integrity was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gibco Dulbecco's Modified Eagle Medium (DMEM) Recalled by Life Technologies,...
The Issue: It has been determined that the fill port tube seal integrity was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gibco RPMI 1640 Medium Recalled by Life Technologies, Corp. Due to It has...
The Issue: It has been determined that the fill port tube seal integrity was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hyalomatrix Recalled by Anika Therapeutics, Inc. Due to Hyalomatrix products...
The Issue: Hyalomatrix products are susceptible to degradation as a result of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: microTargeting" STar" Drive System (Manual) Recalled by FHC, Inc. Due to The...
The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.