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. 1,095 recalls have been distributed to California in the last 12 months.
Showing 27161–27180 of 56,506 recalls
Recalled Item: Levofloxacin Injection in 5% Dextrose Recalled by Baxter Healthcare...
The Issue: Superpotent Drug: High out of specification results for levofloxacin...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levofloxacin Injection in 5% Dextrose Recalled by Baxter Healthcare...
The Issue: Superpotent Drug: High out of specification results for levofloxacin...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ararat Imambayeldy Recalled by Artashes LLC Due to FDA foreign inspection...
The Issue: FDA foreign inspection found pH levels in four products to be above their...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ararat Eggplant Paste 18.3 oz. glass jar Recalled by Artashes LLC Due to FDA...
The Issue: FDA foreign inspection found pH levels in four products to be above their...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ararat Cut Beets Recalled by Artashes LLC Due to FDA foreign inspection...
The Issue: FDA foreign inspection found pH levels in four products to be above their...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ararat Grilled Eggplant and Peppers 23 oz. glass jar Recalled by Artashes...
The Issue: FDA foreign inspection found pH levels in four products to be above their...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sweet Earth Foods Aloha BBQ Quesadilla Recalled by Sweet Earth Inc. Due to...
The Issue: Firm received complaints of Sweet Earth Aloha BBQ Quesadilla packages that...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Alcon Air Optix Night & Day Aqua (lotrafilcon A) Recalled by Allied Vision...
The Issue: Potentially counterfeit products in/and counterfeit packaging were imported...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum 360 Infusion System With MedNet/ Smart Card Plug And Play Module...
The Issue: A software malfunction of the infuser when used with a MedNet Custom Drug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kerlix Bandage Roll Recalled by COVIDIEN LLC Due to Potential for product...
The Issue: Potential for product sterility breach due to a compromised or pinched seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dermacea Gauze Fluff Roll Recalled by COVIDIEN LLC Due to Potential for...
The Issue: Potential for product sterility breach due to a compromised or pinched seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemosll ReadiPlasTin (10 mL Size) Recalled by Instrumentation Laboratory Co....
The Issue: There is a potential for increased imprecision, out of range quality...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kerlix Bandage Roll Recalled by COVIDIEN LLC Due to Potential for product...
The Issue: Potential for product sterility breach due to a compromised or pinched seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dermacea Gauze Fluff Roll Recalled by COVIDIEN LLC Due to Potential for...
The Issue: Potential for product sterility breach due to a compromised or pinched seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kerlix AMD Antimicrobial Bandage Roll Recalled by COVIDIEN LLC Due to...
The Issue: Potential for product sterility breach due to a compromised or pinched seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kerlix Gauze Roll Recalled by COVIDIEN LLC Due to Potential for product...
The Issue: Potential for product sterility breach due to a compromised or pinched seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: sterEOS workstation Recalled by EOS Imaging Due to 3D projections may be...
The Issue: 3D projections may be incorrect when the pair of images used is a secondary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Capnostream20 (US)M Recalled by Oridion Medical 1987 Ltd. Due to The...
The Issue: The date/time, nurse call and alarm settings of the bedside patient monitors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ENDOLOGIX AFX2 Bifurcated Endograft System Recalled by Endologix Due to...
The Issue: Endologix is notifying physicians of patient tailored surveillance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Capnostream20 M ADULT ICU (CPM) Recalled by Oridion Medical 1987 Ltd. Due to...
The Issue: The date/time, nurse call and alarm settings of the bedside patient monitors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.