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. 2,799 recalls have been distributed to California in the last 12 months.
Showing 36201–36220 of 56,506 recalls
Recalled Item: Daytrana (methylphenidate transdermal system) Transdermal Patch Recalled by...
The Issue: Defective Delivery System: Out of Specification (OOS) results for the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Transdermal Patch Recalled by...
The Issue: Defective Delivery System: Out of Specification (OOS) results for the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The EKOS cart has the catalog number 700-60101. The EKOS Recalled by EKOS...
The Issue: Casters on the EKOS carts may be missing washers which can cause premature...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sertera Biopsy Device Recalled by Hologic, Inc Due to Incorrect label on the...
The Issue: Incorrect label on the Sertera Biopsy Kit
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lamotrigine Orally Disintegrating Tablets (ODT) Recalled by Impax...
The Issue: Labeling; Label Mixup; box labeled to contain 200 mg blister packs but...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lamotrigine Tablets Recalled by Unichem Pharmaceuticals Usa Inc Due to...
The Issue: Tablets/Capsules Imprinted With Wrong ID: incorrect imprint debossed on the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Panoramic X-ray Model PC-1000 Recalled by Panoramic Rental Corp. Due to...
The Issue: Panoramic Corporation is performing a voluntary Medical Device Correction on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amoxicillin For Oral Suspension Recalled by West-Ward Pharmaceuticals Corp....
The Issue: Labeling: Label Error on Declared Strength- bottles missing colored coded...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Frozen Raw Bay Scallops Recalled by Sea Port Products Corp Due to Frozen Raw...
The Issue: Frozen Raw Bay scallops are recalled due to a potential contamination with...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: HexaPOD evo RT System Product Usage: The intended use of Recalled by Elekta,...
The Issue: Potentially unrecognized incorrect position of the treatment couch in 3D...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monaco RTP System Used to make treatment plans for patients Recalled by...
The Issue: In a specific workflow where contours are edited (enlarged, moved, copied,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIO-A / NIO-P is an instant IO access device comprises Recalled by Waismed...
The Issue: WaisMed received a report in which during the operation of the NIO-A, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sagittal Blade 18.0X0.97X90MM Recalled by Stryker Instruments Div. of...
The Issue: Stryker Instruments is voluntarily recalling the Sagittal Blade...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare Ventricular Assist System (HVAD) Recalled by HeartWare, Inc Due to...
The Issue: Foreign material found within the driveline connector of the HVAD Pump that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Honeywell eyesaline Eyewash Sterile Isotonic Solution Recalled by Sperian...
The Issue: Non Sterility; contaminated with Klebsiella pneumoniae
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Croissant Recalled by Bakers Of Paris, Inc. Due to Labeling for Croissants...
The Issue: Labeling for Croissants and Chocolate Croissants fails to declare egg in the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Chocolate Croissant Recalled by Bakers Of Paris, Inc. Due to Labeling for...
The Issue: Labeling for Croissants and Chocolate Croissants fails to declare egg in the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Coonrad/ Morrey Elbow Pin/ Bushing Replacement size Kit Extra Small....
The Issue: Zimmer Biomet is conducting a voluntary medical device recall of a single...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DOBUTamine Injection Recalled by Hospira Inc. Due to Discoloration: Firm...
The Issue: Discoloration: Firm received complaints of product discoloration and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pentax Video Colonoscope is intended to be used with a Recalled by Pentax of...
The Issue: Pentax is initiating the product correction of several model numbers of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.