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Latest Product Recalls Today

Track recent product recall alerts from official U.S. sources. Filter by recall date, source agency, risk level and product category to find newly published food, vehicle, baby product, medical device and consumer product recalls.

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Search recent recall notices by product name, brand, UPC, lot code, model number, source agency or official recall number.

Recent Product Recall Alerts List

Showing 2,276 - 2,300 of 3,321 matching product recalls.
Product Recall Search
Product Recall Source Type Risk Date Action
GEM Premier 5000; Part No. 00055430008.
Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution Not Detected (PCSND) errors during warm-up, including consecutive occurrences, resulting in GEM PAK ejection and requiring insertion of a new GEM PAK. iQM2 is an active quality process control program designed to provide continuous monitoring of the entire testing process. Thus, if a GEM PAK completes AutoPAK Validation following warm-up, it may remain in use. Consecutive GEM PAK ejections during warm-up may prolong turnaround times, potentially delaying results. In such cases, patient management may require reassessment once results are available. While many GEM PAKs continue to perform as intended, consecutive ejections may increase the likelihood of operational disruption, highlighting the importance of advance planning where feasible to help minimize impact.
FDA Z-1538-2026
Medical Device High
Mar 18, 2026 Recall: Jan 20, 2026
Details
GEM Premier 5000; Model No. 00055430010.
Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution Not Detected (PCSND) errors during warm-up, including consecutive occurrences, resulting in GEM PAK ejection and requiring insertion of a new GEM PAK. iQM2 is an active quality process control program designed to provide continuous monitoring of the entire testing process. Thus, if a GEM PAK completes AutoPAK Validation following warm-up, it may remain in use. Consecutive GEM PAK ejections during warm-up may prolong turnaround times, potentially delaying results. In such cases, patient management may require reassessment once results are available. While many GEM PAKs continue to perform as intended, consecutive ejections may increase the likelihood of operational disruption, highlighting the importance of advance planning where feasible to help minimize impact.
FDA Z-1539-2026
Medical Device High
Mar 18, 2026 Recall: Jan 20, 2026
Details
FDA Z-1498-2026
Medical Device High
Mar 18, 2026 Recall: Jan 5, 2026
Details
Endo-Model SL Connection Component incl. PE-Plateau; Item Number: 16-2840/05;
The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.
FDA Z-1511-2026
Medical Device High
Mar 18, 2026 Recall: Jan 12, 2026
Details
Owner's Booklets and Instructions for Use that are used with the following blood glucose measuring devices. Description/Item: Walgreens TRUE METRIX AIR Kit/REA4001-01, Leader TRUE METRIX AIR Kit/REA4002-01, CVS TRUE METRIX AIR Kit/REA4007-01, GNP TRUE METRIX AIR Kit/REA4011-01, Meijer TRUE METRIX AIR Kit/REA4019-01, Publix TRUE METRIX AIR Kit/REA4020-01, Discount Drug Mart TRUE METRIX AIR Kit/REA4025-01, HEB TRUE METRIX AIR Kit/REA4031-01, SunmarkTRUE METRIX AIR Kit/REA4054-01, Rite AidTRUE METRIX AIR Kit/REA4066-01, Centerwell TRUE METRIX AIR Kit/REA4081-01, HumanaTRUE METRIX AIR Meter Only/R
The system labeling (user manual and online labeling) did not provide adequate directions for lay users to act on the E-5 error code. The error code description and recommended actions for the E-5 error code in the labeling do not: (a) clearly emphasize that an E-5 error code could represent a very high blood glucose level, and (b) prominently convey the appropriate immediate actions, such as contacting a healthcare professional. This could lead to a delay in treatment if the user does not seek medical attention immediately when receiving an E-5 error code and experiencing symptoms of high glucose.
FDA Z-1547-2026
Medical Device High
Mar 18, 2026 Recall: Feb 6, 2026
Details
Endo-Model Replacement Plateau; Item Number: 15-8030/12;
The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.
FDA Z-1517-2026
Medical Device High
Mar 18, 2026 Recall: Jan 12, 2026
Details
GEM Premier 5000; Part No. 00055415005.
Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution Not Detected (PCSND) errors during warm-up, including consecutive occurrences, resulting in GEM PAK ejection and requiring insertion of a new GEM PAK. iQM2 is an active quality process control program designed to provide continuous monitoring of the entire testing process. Thus, if a GEM PAK completes AutoPAK Validation following warm-up, it may remain in use. Consecutive GEM PAK ejections during warm-up may prolong turnaround times, potentially delaying results. In such cases, patient management may require reassessment once results are available. While many GEM PAKs continue to perform as intended, consecutive ejections may increase the likelihood of operational disruption, highlighting the importance of advance planning where feasible to help minimize impact.
FDA Z-1533-2026
Medical Device High
Mar 18, 2026 Recall: Jan 20, 2026
Details
Artelon FlexBand Dynamic Matrix Ref: 31057
Augmentation devices failed bacterial endotoxin testing.
FDA Z-1554-2026
Medical Device High
Mar 18, 2026 Recall: Feb 6, 2026
Details
Owner's Booklets and Instructions for Use that are used with the following blood glucose measurement devices. Description/Item: TRUE METRIX PRO Meter Only/RE4H01P-40, TRUE METRIX PRO Starter Kit/RE4H01P-43, PROCURE TRUE METRIX PRO Meter Only/RE4212P-00, Henry Schein TRUE METRIX PRO Meter Only/RE4099P-40, Henry Schein TRUE METRIX PRO Kit/RE4099P-43, McKESSON TRUE METRIX PRO Meter Only/RE4051P-00, Moore Medical TRUE METRIX PRO Meter Only/RE4068P-01.
The system labeling (user manual and online labeling) did not provide adequate directions for lay users to act on the E-5 error code. The error code description and recommended actions for the E-5 error code in the labeling do not: (a) clearly emphasize that an E-5 error code could represent a very high blood glucose level, and (b) prominently convey the appropriate immediate actions, such as contacting a healthcare professional. This could lead to a delay in treatment if the user does not seek medical attention immediately when receiving an E-5 error code and experiencing symptoms of high glucose.
FDA Z-1546-2026
Medical Device High
Mar 18, 2026 Recall: Feb 6, 2026
Details
CHEMISTRY ANALYZER AU5800, REF: B96697, B96698, B23279, B23280, B23281
A delay in results may occur. When clinical chemistry analyzer calibration monitor with PC installed with Microsoft SQL Server 2022 Express is open beyond15 minutes may lead to: Reagent Blank and calibration databases not opening errors: CAL History DB Open Error.., RB History DB Open Error..; system will stop analyzing, firm service must visit to apply software solution; may lead to delay in diagnosis and/or patient treatment
FDA Z-1553-2026
Medical Device High
Mar 18, 2026 Recall: Jan 30, 2026
Details
GEM Premier 5000 PAK, Part No. 00055360004.
Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution Not Detected (PCSND) errors during warm-up, including consecutive occurrences, resulting in GEM PAK ejection and requiring insertion of a new GEM PAK. iQM2 is an active quality process control program designed to provide continuous monitoring of the entire testing process. Thus, if a GEM PAK completes AutoPAK Validation following warm-up, it may remain in use. Consecutive GEM PAK ejections during warm-up may prolong turnaround times, potentially delaying results. In such cases, patient management may require reassessment once results are available. While many GEM PAKs continue to perform as intended, consecutive ejections may increase the likelihood of operational disruption, highlighting the importance of advance planning where feasible to help minimize impact.
FDA Z-1524-2026
Medical Device High
Mar 18, 2026 Recall: Jan 20, 2026
Details
Penner Pacific Bathing Spa, Model Numbers 360020-1P
The device does not bear a unique device identifier.
FDA Z-1502-2026
Medical Device High
Mar 18, 2026 Recall: Aug 13, 2025
Details
Endo-Model Replacement Plateau; Item Number: 15-0027/11;
The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.
FDA Z-1521-2026
Medical Device High
Mar 18, 2026 Recall: Jan 12, 2026
Details
Made Fresh Salads brand Caramel Apple Cream Cheese; 5 lb white plastic tub
Products may be contaminated with Listeria monocytogenes.
FDA H-0556-2026
Food High
Mar 18, 2026 Recall: Feb 19, 2026
Details
Made Fresh Salads brand Sundried Tomato Cream Cheese; 5 lb white plastic tub
Products may be contaminated with Listeria monocytogenes.
FDA H-0564-2026
Food High
Mar 18, 2026 Recall: Feb 19, 2026
Details
Made Fresh Salads brand Tofu Whipped; 5 lb white plastic tub
Products may be contaminated with Listeria monocytogenes.
FDA H-0568-2026
Food High
Mar 18, 2026 Recall: Feb 19, 2026
Details
FDA H-0548-2026
Food High
Mar 18, 2026 Recall: Jan 17, 2026
Details
FDA H-0546-2026
Food High
Mar 18, 2026 Recall: Feb 13, 2026
Details
FDA H-0549-2026
Food High
Mar 18, 2026 Recall: Feb 9, 2026
Details
FDA H-0614-2026
Food High
Mar 18, 2026 Recall: Mar 2, 2026
Details
Made Fresh Salads brand Jalapeno Cheddar Cream Cheese; 5 lb white plastic tub
Products may be contaminated with Listeria monocytogenes.
FDA H-0560-2026
Food High
Mar 18, 2026 Recall: Feb 19, 2026
Details
Made Fresh Salads brand Walnut Raisin Cream Cheese; 5 lb white plastic tub
Products may be contaminated with Listeria monocytogenes.
FDA H-0566-2026
Food High
Mar 18, 2026 Recall: Feb 19, 2026
Details
Made Fresh Salads brand Jalapeno Cream Cheese; 5 lb white plastic tub
Products may be contaminated with Listeria monocytogenes.
FDA H-0559-2026
Food High
Mar 18, 2026 Recall: Feb 19, 2026
Details
C2O Coconut Water with Pulp (17.5 oz) 15 Pack UPC: 8-50274-00792-8
The outer cardboard box for the canned coconut water has the incorrect Nutrition Facts Panel and Ingredient List, which does not include added sugar (5g per 17.5oz can), while the primary packaging (the can) has the correct Nutrition Facts Panel and Ingredient List.
FDA H-0545-2026
Food High
Mar 18, 2026 Recall: Feb 25, 2026
Details
FDA H-0553-2026
Food High
Mar 18, 2026 Recall: Feb 3, 2026
Details
Showing 2,276 - 2,300 of 3,321 product recalls

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NHTSA

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