Product Recalls in New York
Product recalls affecting New York — including food, drugs, consumer products, medical devices, and vehicles distributed to New York. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,771 recalls have been distributed to New York in the last 12 months.
Showing 16221–16240 of 30,153 recalls
Recalled Item: CE18TOD CONT EPIDURAL TRAY LF Recalled by B. Braun Medical, Inc. Due to The...
The Issue: The catheter connectors may not stay closed during in and in some cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLAMP STYLE CATH. CONNECTOR 18-19 GA- LF Recalled by B. Braun Medical, Inc....
The Issue: The catheter connectors may not stay closed during in and in some cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CE17TOD CONT EPIDURAL TRAY LF Recalled by B. Braun Medical, Inc. Due to The...
The Issue: The catheter connectors may not stay closed during in and in some cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CE17TKFPS PERIFIX FX CONT. EPID TRAY-LF Recalled by B. Braun Medical, Inc....
The Issue: The catheter connectors may not stay closed during in and in some cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GOVCE18TK ACCU-BLOC PERIFIX KIT Recalled by B. Braun Medical, Inc. Due to...
The Issue: The catheter connectors may not stay closed during in and in some cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CE17TKFMHDT 17 GA X 4 FULL EPID KIT Recalled by B. Braun Medical, Inc. Due...
The Issue: The catheter connectors may not stay closed during in and in some cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CE17TB19C CONT EPIDURAL TRAY Recalled by B. Braun Medical, Inc. Due to The...
The Issue: The catheter connectors may not stay closed during in and in some cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beaver Accu-Temp High Temperature Cautery Recalled by Beaver Visitec Due to...
The Issue: A small number of devices in this lot may have a melted cap and a hole...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott ARCHITECT Creatine Kinase Recalled by Abbott Laboratories, Inc Due to...
The Issue: The product has a stability issue which may lead to an error code indicating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott ARCHITECT Creatine Kinase Recalled by Abbott Laboratories, Inc Due to...
The Issue: The product has a stability issue which may lead to an error code indicating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott ARCHITECT c16000 Processing Module Recalled by Abbott Laboratories,...
The Issue: There is a potential to generate incorrect results on the instrument if...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott ARCHITECT c4000 Processing Module Recalled by Abbott Laboratories,...
The Issue: There is a potential to generate incorrect results on the instrument if...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott ARCHITECT c8000 Processing Module Recalled by Abbott Laboratories,...
The Issue: There is a potential to generate incorrect results on the instrument if...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alcon or Endure Ophthalmic Microscope Product Usage: Used for low Recalled...
The Issue: Potential for the optical head to detach from the stand due to the lack of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4.5 Fr x 40 cm single-lumen PICC Kit Recalled by Arrow International Inc Due...
The Issue: The products may contain the incorrect catheter. Kits that should contain a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus¿ Hip Fracture Nail Right 130¿ 11 mm x 440 mm Recalled by Zimmer...
The Issue: The set screw is not able to advance or reverse from the original position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus¿ Hip Fracture Nail Right 125¿ 13 mm x 440 mm Recalled by Zimmer...
The Issue: The set screw is not able to advance or reverse from the original position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus¿ Hip Fracture Nail Right 130¿ 11 mm x 320 mm Recalled by Zimmer...
The Issue: The set screw is not able to advance or reverse from the original position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5.5 Fr x 40 cm double-lumen PICC Kit Recalled by Arrow International Inc Due...
The Issue: The products may contain the incorrect catheter. Kits that should contain a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus¿ Hip Fracture Nail Right 125¿ 9 mm x 440 mm Recalled by Zimmer...
The Issue: The set screw is not able to advance or reverse from the original position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.