State

New York product recalls

73,366 recalls have nationwide distribution and so reach New York. 12,941 additional recalls listed New York specifically in their distribution scope.

What the numbers show

Total: 12,941
Critical: 1,511
Severe: 3,698
Most recent: 2026-10-07

Of the 12,941 recalls naming New York we have scored against our rubric, 1,511 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 3,698 (29%) are Severe.

Which agencies issued them

These figures cover only the 12,941 recalls whose distribution notice names New York specifically. The 73,366 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

18551–18575 of 86307

HighFDA (Devices)·Z-1560-2023·2023-05-10
Laboratory Automation System Firmware May Misassociate Patient Samples
Inpeco laboratory automation systems have a firmware defect that may cause sample ID mis-association, leading to incorrect test results for electrolyte measurements. Potential consequences include abnormal treatment decisions and serious health complications.
Product
Storage and Retrieval Module (SRM)-Laboratory Automation system Brand names of the same product: FlexLab (FLX), Accelerator a3600 (ACP), Aptio Automation (AP2) Part Numbers: ACP-207-00, ACP-207-01, ACP-230-00, ACP-230-01 APT-207-00, APT-207-01, APT-230-00, APT-230-01…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1552-2023·2023-05-10
Knee Implant Recall for Aseptic Loosening and Implant Wear Risk
The LINK SLED Knee System is recalled due to risk of early aseptic loosening and implant wear caused by suboptimal surgical positioning or inadequate cementing. The manufacturer is updating surgical guidance and providing additional training.
Product
LINK SLED Knee System POREX ENDO MODEL SLED TIBIAL COMP 8 MM X 45 MM Item Number: 15-2230/13
Category
Medical Device
Distribution
2 states
HighFDA (Devices)·Z-1530-2023·2023-05-10
LINK SLED Knee Implant Recall: Risk of Early Loosening and Revision Surgery
Linkbio Corp. is recalling 14 LINK SLED Knee implants due to risk of aseptic loosening and increased wear caused by improper surgical technique. The implants may fail earlier than expected, requiring revision surgery.
Product
LINK SLED Knee System ENDO MODEL SLED TIBIAL COMP 9 MM X 50 MM Item Number: 15-2030/06
Category
Medical Device
Distribution
2 states
HighFDA (Food)·F-0809-2023·2023-05-10
Atkins Dark Chocolate Royale Protein Shakes Recalled for Contamination
Simply Good Foods Co. is recalling Atkins Dark Chocolate Royale Protein Rich Shakes due to contamination that rendered the product non-sterile, creating potential for spoilage.
Product
Atkins Dark Chocolate Royale Protein Rich Shakes, NET WT. 44 oz (4 / 11oz) 4 Tetra packs per carton, UPC 637480065108, Distributed exclusively by Simply Good Foods USA, Inc. 1 Denver, CO 80202 1-800-6-ATKINS.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1554-2023·2023-05-10
LINK SLED Knee System tibial implant recalled for aseptic loosening
Linkbio Corp. recalls LINK SLED Knee System tibial component due to risk of aseptic loosening and implant wear from improper surgical technique, potentially requiring revision surgery.
Product
LINK SLED Knee System POREX ENDO MODEL SLED TIBIAL COMP 8 MM X 55 MM Item Number: 15-2230/15
Category
Medical Device
Distribution
2 states
HighFDA (Devices)·Z-1548-2023·2023-05-10
LINK SLED knee implant system surgical technique amendment for aseptic loosening prevention
Linkbio Corp. is updating surgical technique guidance for the LINK SLED knee implant system to prevent early aseptic loosening or implant wear caused by suboptimal positioning or cementing technique during surgery.
Product
LINK SLED Knee System POREX ENDO MODEL SLED TIBIAL COMP 13 MM X 50 MM Item Number: 15-2230/08
Category
Medical Device
Distribution
2 states
HighFDA (Devices)·Z-1540-2023·2023-05-10
LINK SLED Knee System recalls issued over aseptic loosening risk
Linkbio Corp. is recalling LINK SLED Knee System knee components due to risk of early aseptic loosening or increased wear. The company is issuing updated surgical technique guidance to address suboptimal implant positioning and cementing techniques.
Product
LINK SLED Knee System POREX ENDO SLED KNEE FEM COMP, MEDIUM SMALL Item Number: 15-2220/46
Category
Medical Device
Distribution
2 states
HighFDA (Devices)·Z-1513-2023·2023-05-10
Knee Implant System Component Recalled Due to Aseptic Loosening Risk
Linkbio Corp. is recalling 13 units of the LINK SLED Knee System tibial component due to risk of aseptic loosening and increased wear. These risks arise from improper surgical positioning or inadequate cementing technique during implantation.
Product
LINK SLED Knee System: ALL POLY TIBIAL COMPONENT 11MM X 45MM Item Number: 15-2028/03
Category
Medical Device
Distribution
2 states
HighFDA (Devices)·Z-1510-2023·2023-05-10
LINK SLED knee implant system recalled for inadequate surgical technique
Linkbio Corp. is amending training for the LINK SLED Knee System due to early implant loosening and wear caused by inadequate surgical positioning and cementing techniques. Healthcare providers should implement updated surgical guidance.
Product
LINK SLED Knee System: ENDO SLED KNEE FEM COMP, Large Item Number: 15-2020/60
Category
Medical Device
Distribution
2 states
HighFDA (Devices)·Z-1535-2023·2023-05-10
Knee Implant Recalled for Inadequate Surgical Technique Guidance
Linkbio is recalling 15 LINK SLED Knee Systems due to potential aseptic loosening and wear from suboptimal implant positioning or inadequate cementing during surgery. Updated surgical technique training is required.
Product
LINK SLED Knee System ENDO MODEL SLED TIBIAL COMP 13 MM X 55 MM Item Number: 15-2030/12
Category
Medical Device
Distribution
2 states
HighFDA (Devices)·Z-1526-2023·2023-05-10
LINK SLED Knee Implant System recalled for early aseptic loosening
The LINK SLED Knee System ALL POLY TIBIAL COMPONENT (18 units) is recalled due to early aseptic loosening and increased wear caused by suboptimal positioning or inadequate cementing technique, which may require earlier-than-expected revision surgery.
Product
LINK SLED Knee System: ALL POLY TIBIAL COMPONENT 13X58MM Item Number: 15-2028/16
Category
Medical Device
Distribution
2 states
HighFDA (Food)·F-0781-2023·2023-05-10
Prolia soy flour products recalled for undisclosed gluten content
Cargill is recalling multiple PROLIA soy flour products that carry gluten-free claims but may contain gluten above 20 ppm. Consumers with celiac disease or gluten sensitivity should not consume affected products.
Product
PROLIA SOY FLR 200/20 STD BLK, PROLIA SOY FLR 200/70 STD BLK, PROLIA SOY FLR 300/70 NT BLK, PROLIA SOY FLR 100/20 STD 1MT TT, PROLIA SOY FLR 100/90 STD 1500LB TT, PROLIA SOY FLR 100/90 NT 50LB BG, PROLIA SOY FLR 200/20 XTRA 50LB BG NGM, PROLIA SOY FLR 200/20 STD 50LB BG, PROLIA…
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1504-2023·2023-05-10
Siemens Atellica cortisol kits recalled for negative bias in urine testing
Siemens Healthcare Diagnostics recalls 34,746 Atellica IM Cortisol diagnostic kits due to negative bias in urine test results, which may produce inaccurately low cortisol measurements.
Product
Atellica IM Cortisol 50T (Material Number 10995538), 250T (Material Number 10995537), and REF 250T (Material Number 11206248). In vitro diagnostic use in the quantitative determination of cortisol in human serum, plasma (EDTA and lithium heparin), and urine.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1563-2023·2023-05-10
Laboratory automation system firmware recalled for sample mis-identification
Inpeco is recalling Alinity h laboratory automation system firmware that may mis-identify samples, causing incorrect electrolyte test results that could lead to improper patient treatment.
Product
Alinity h Interface Module (HSQ)-Laboratory Automation system Brand names of the same product: FlexLab (FLX), Accelerator a3600 (ACP), Aptio Automation (AP2) Part Numbers: FLX-274-20
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0793-2023·2023-05-10
Soy Flour Recalled for Undisclosed Gluten Levels
Cargill is recalling PROSANTE TSOYFLR soy flour labeled as gluten-free that may contain gluten exceeding safe limits (20 ppm). The product was distributed nationwide and internationally.
Product
PROSANTE TSOYFLR 12P MNCD 50LB BG/36P, paper bag
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0791-2023·2023-05-10
Cargill Gluten-Free Product Recall Due to Gluten Content
Cargill is recalling approximately 110,650 pounds of PROSANTE TVGPTN 12B products labeled as gluten-free because they may contain gluten above the safe threshold.
Product
PROSANTE TVGPTN 12B MNCD 50LB BG, PROSANTE TVGPTN 12B MNCD 50LB BG 21/P, paper bag
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1534-2023·2023-05-10
Knee implant system recalled due to risk of aseptic loosening
The LINK SLED Knee System has been recalled due to risk of early aseptic loosening and wear caused by suboptimal implant positioning or inadequate cementing technique during surgery.
Product
LINK SLED Knee System ENDO MODEL SLED TIBIAL COMP 11 MM X 55 MM Item Number: 15-2030/11
Category
Medical Device
Distribution
2 states
HighFDA (Devices)·Z-1531-2023·2023-05-10
LINK SLED Knee Implant Recall Due to Loosening and Wear Risks
Linkbio Corp. is recalling 14 units of LINK SLED Knee System implants due to risk of early aseptic loosening or wear from suboptimal positioning or inadequate cementing. Updated surgical technique training is being issued.
Product
LINK SLED Knee System ENDO MODEL SLED TIBIAL COMP 11 MM X 50 MM Item Number: 15-2030/07
Category
Medical Device
Distribution
2 states
HighFDA (Devices)·Z-1522-2023·2023-05-10
Knee Implant Component Recalled for Aseptic Loosening Risk
Linkbio Corp. recalls 14 units of the LINK SLED Knee System tibial component due to risk of early aseptic loosening and increased wear from suboptimal implant positioning or inadequate cementing technique. Healthcare providers should follow updated surgical guidance.
Product
LINK SLED Knee System: ALL POLY TIBIAL COMPONENT 13MM X 55MM Item Number: 15-2028/12
Category
Medical Device
Distribution
2 states
HighFDA (Food)·F-0780-2023·2023-05-10
Soy Flour Products Recalled for Potential Gluten Contamination
Cargill recalls 977,000 pounds of soy flour products labeled gluten-free that may contain gluten above FDA limits. Products were distributed in the US and multiple countries.
Product
PROSANTE TSOYFLR 3018P FLK 50LB BG, PROSANTE TSOYFLR 3018P FLK 50LB BG 18/P, PROSANTE TSOYFLR 3018P FLK 25LB BG/36, paper bag
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0795-2023·2023-05-10
Cargill Prosante Grain Products Recalled for Undeclared Gluten Content
Cargill is recalling 36,000 lbs of grain products labeled as gluten-free that may contain gluten above the FDA safety limit. Consumers with celiac disease or gluten sensitivity should not consume affected product code 110026470-02523CHXEA.
Product
PROSANTE TVGPTN 10PF MNCD 50LB BG/36P, paper bag
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1553-2023·2023-05-10
Knee Implant System Warning: Risk of Early Loosening Due to Surgical Technique
Linkbio Corp. is updating labeling and surgical technique training for the LINK SLED Knee System to prevent early aseptic loosening or excessive wear caused by improper implant positioning or inadequate cementing during surgery.
Product
LINK SLED Knee System POREX ENDO MODEL SLED TIBIAL COMP 8 MM X 50 MM Item Number: 15-2230/14
Category
Medical Device
Distribution
2 states
HighFDA (Food)·F-0796-2023·2023-05-10
Soybean Flour Recalled for Potential Undeclared Gluten
Cargill is recalling PROSANTE soybean flour products that may contain gluten levels exceeding 20 ppm despite gluten-free labeling. Approximately 826,150 pounds were distributed nationwide and internationally.
Product
PROSANTE SOYFLR 3038P FLK 50LB BG, PROSANTE TSOYFLR 3038P FLK 50LB BG/18P, paper bags
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1528-2023·2023-05-10
LINK SLED Knee System tibial component recall for aseptic loosening and wear risk
Linkbio Corp. is recalling 15 units of the LINK SLED Knee System tibial component for risk of aseptic loosening and wear from improper implant positioning or inadequate cementing technique. Surgical training will be updated.
Product
LINK SLED Knee System: ENDO MODEL SLED TIBIAL COMP 11 MM X 45 MM Item Number: 15-2030/03
Category
Medical Device
Distribution
2 states
HighFDA (Devices)·Z-1515-2023·2023-05-10
LINK SLED Knee Implant Tibial Component: Surgical Technique Amendment
Linkbio Corp. is issuing updated surgical technique guidance and training for the LINK SLED Knee System tibial component due to risk of early implant loosening or wear from suboptimal positioning or inadequate cementing.
Product
LINK SLED Knee System: ALL POLY TIBIAL COMPONENT 7MM X 50MM Item Number: 15-2028/05
Category
Medical Device
Distribution
2 states