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. 2,581 recalls have been distributed to New York in the last 12 months.
Showing 40501–40520 of 55,896 recalls
Recalled Item: Model 5001102 MPS Delivery Set w/ arrest agent and additive cassettes...
The Issue: The products have been found to intermittently exhibit a seal failure during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: rainbow Reusable Sensors. RAINBOW DCI-DC3 Recalled by Masimo Corporation Due...
The Issue: These sensors were manufactured with incompatible configurations. This could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProTrack Microcatheter. Model/Catalog Numbers CIC38-145 Recalled by Baylis...
The Issue: Microcatheter may have circumferential defects (cracks) along its shaft.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DA-2006P - Defibrillator / Pacer Analyzer Recalled by BC Group International...
The Issue: Device is not functioning as intended: Two wires running to the ECG...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Perfusion Tubing Packs Recalled by Medtronic Perfusion Systems Due...
The Issue: This recall is being initiated due to a potential breach of the Tubing Pack...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Auvi-Q (epinephrine injection Recalled by Sanofi-Aventis U.S. LLC Due to...
The Issue: Defective Delivery System; potential to have inaccurate dosage delivery
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Auvi-Q (epinephrine injection Recalled by Sanofi-Aventis U.S. LLC Due to...
The Issue: Defective Delivery System; potential to have inaccurate dosage delivery
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GRx HiCort 25 (hydrocortisone acetate 25 mg) Suppositories Recalled by...
The Issue: Marketed without an Approved NDA/ANDA: FDA has determined that the products...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carbo-O-Philic 40 Gel 40% (Urea) NET WT tube Recalled by Geritrex Corp Due...
The Issue: Marketed without an Approved NDA/ANDA: FDA has determined that the products...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Polyethylene Glycol 3350-GRX Powder 100% jars a) 8.4 oz (250 Recalled by...
The Issue: Marketed without an Approved NDA/ANDA: FDA has determined that the products...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carbo-O-Philic 40 Cream 40% (Urea) tubes Recalled by Geritrex Corp Due to...
The Issue: Marketed without an Approved NDA/ANDA: FDA has determined that the products...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Doria AUTHENTIC ITALIAN GOODNESS Recalled by Bauli Due to Bauli S.p.A. has...
The Issue: Bauli S.p.A. has initiated a recall due to high levels of Aflatoxin B1
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Herr's Sour Cream & Onion Flavored Potato Chips Recalled by Herrs Foods Inc...
The Issue: Herr Foods Inc. has initiated a voluntary recall of certain bags of its...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: U-SDN 2 Part Ultra Modified Seldinger Needles Recalled by Procedure...
The Issue: The firm had received a complaint alleging that a medical professional had...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IOL Master 5.5: Software versions 7.5 and 7.7 Recalled by Carl Zeiss Meditec...
The Issue: IOL Master software versions 7.5 and 7.7 calculation printouts and exported...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IOL Master 500: Software versions 7.5 and 7.7 Recalled by Carl Zeiss Meditec...
The Issue: IOL Master software versions 7.5 and 7.7 calculation printouts and exported...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROLARYN PLUS Injectable Implant 1.0 cc Plus Calcium Hydroxlyapatite (CaHA)...
The Issue: The expiration date encoded in the UDI barcode on the label on the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniArc Pro Single incision Sling System Recalled by Astora Due to The lot...
The Issue: The lot number on the outer carton label did not match the lot number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROLARYN Injectable Implant 1.0 cc Gel Recalled by Merz North America, Inc....
The Issue: The expiration date encoded in the UDI barcode on the label on the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radiesse (+) Lidocaine Injectable Implant 1.5cc Recalled by Merz North...
The Issue: The expiration date encoded in the UDI barcode on the label on the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.