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. 2,659 recalls have been distributed to New York in the last 12 months.
Showing 26221–26240 of 30,153 recalls
Recalled Item: Methamphetamine Test Card Recalled by LumiQuick Diagnostics Inc. Due to...
The Issue: Products shipped to US locations that do not have approved applications for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adenovirus Antigen Test Card Recalled by LumiQuick Diagnostics Inc. Due to...
The Issue: Products shipped to US locations that do not have approved applications for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Benzodiazepine Strip Recalled by LumiQuick Diagnostics Inc. Due to Products...
The Issue: Products shipped to US locations that do not have approved applications for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fecal Occult Blood Test Strip Recalled by LumiQuick Diagnostics Inc. Due to...
The Issue: Products shipped to US locations that do not have approved applications for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cocaine Test Card Recalled by LumiQuick Diagnostics Inc. Due to Products...
The Issue: Products shipped to US locations that do not have approved applications for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Methylphenidate Test Strip Recalled by LumiQuick Diagnostics Inc. Due to...
The Issue: Products shipped to US locations that do not have approved applications for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amphetamine Strip Recalled by LumiQuick Diagnostics Inc. Due to Products...
The Issue: Products shipped to US locations that do not have approved applications for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ketamine Strip Recalled by LumiQuick Diagnostics Inc. Due to Products...
The Issue: Products shipped to US locations that do not have approved applications for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Salmonella typhi Antigen Test Card Recalled by LumiQuick Diagnostics Inc....
The Issue: Products shipped to US locations that do not have approved applications for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tramadol Strip Recalled by LumiQuick Diagnostics Inc. Due to Products...
The Issue: Products shipped to US locations that do not have approved applications for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Barbiturate Strip Recalled by LumiQuick Diagnostics Inc. Due to Products...
The Issue: Products shipped to US locations that do not have approved applications for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxycodone Strip Recalled by LumiQuick Diagnostics Inc. Due to Products...
The Issue: Products shipped to US locations that do not have approved applications for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EDDP Test Card Recalled by LumiQuick Diagnostics Inc. Due to Products...
The Issue: Products shipped to US locations that do not have approved applications for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Morph AccessPro Steerable Introducer Recalled by Biocardia, Inc. Due to Firm...
The Issue: Firm discovered the potential for particulates in the inner lumen of Morph...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Dual-stage Venous Return Cannulae Recalled by Terumo Cardiovascular...
The Issue: During in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Malleable Dual-stage Venous Return Cannulae Recalled by Terumo...
The Issue: During in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Malleable Dual-stage Venous Return Cannulae Recalled by Terumo...
The Issue: During in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Malleable Dual-stage Venous Return Cannulae Recalled by Terumo...
The Issue: During in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Dual-stage Venous Return Cannulae Recalled by Terumo Cardiovascular...
The Issue: During in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Malleable Dual-stage Venous Return Cannulae Recalled by Terumo...
The Issue: During in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.