State

Missouri product recalls

73,824 recalls have nationwide distribution and so reach Missouri. 8,501 additional recalls listed Missouri specifically in their distribution scope.

What the numbers show

Total: 8,501
Critical: 1,339
Severe: 2,204
Most recent: 2026-11-04

Of the 8,501 recalls naming Missouri we have scored against our rubric, 1,339 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,204 (26%) are Severe.

Which agencies issued them

These figures cover only the 8,501 recalls whose distribution notice names Missouri specifically. The 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

49601–49625 of 82325

HighFDA (Devices)·Z-1173-2017·2017-03-01
Biomet Oxford Knee Instruments Recalled for Potential Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Phase 3 Tibial Template Right Medial Size C Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1159-2017·2017-03-01
Biomet Oxford Partial Knee Instruments Recalled for Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Left Medial Tibial Trial Tray Size A Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Food)·F-1527-2017·2017-03-01
Falafel King Recalls Tzatziki Sauce for Undeclared Milk Allergen
Falafel King is recalling 1,380 containers of Tzatziki Sauce due to undeclared milk on the label. The product was distributed in Colorado, New Mexico, Utah, and Nebraska.
Product
Falafel King Tzatziki Sauce. 10 ounce. Plastic container
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1170-2017·2017-03-01
Biomet Recalls Oxford Knee Instruments Due to Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Unicompartmental Knee Phase 3 Shim Size 1 instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Unicompartmental Knee Phase 3 Shim Size 1 Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1158-2017·2017-03-01
Biomet Recalls Oxford Knee Instruments Due to Material Inclusions
Biomet is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Right Medial Tibial Trial Tray Size A Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighNHTSA·17V127000·2017-03-01
Volvo Recalls 2017 Models for Side Air Bag Inflator Defect
Volvo is recalling 2017 S60, V60, and XC60 vehicles because side air bag inflators may fail to ignite, preventing deployment in a crash.
Product
VOLVO — VOLVO V60, XC60, S60, V60CC
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1169-2017·2017-03-01
Biomet Recalls Oxford Knee Instruments Due to Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Knee instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Unicompartmental Knee Phase 3 Shim Size 2 Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1154-2017·2017-03-01
Biomet Recalls Oxford Knee Instruments Due to Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Knee instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Unicompartmental Knee Phase 3 Tibial Impactor Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1162-2017·2017-03-01
Biomet Oxford Partial Knee Instruments Recalled for Material Inclusions
Biomet is recalling Oxford Partial Knee instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Right Medial Tibial Trial Tray Size D Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1160-2017·2017-03-01
Biomet Oxford Knee Instruments Recalled for Material Inclusions
Biomet is recalling Oxford Partial Knee instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Right Medial Tibial Trial Tray Size E Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighNHTSA·17V129000·2017-03-01
Forest River Recalls 2017 Rockwood and Flagstaff Trailers for Tire Defect
Forest River is recalling 2017 Rockwood and Flagstaff recreational trailers because a slide room bracket may damage the front tire, causing deflation and increasing crash risk.
Product
FOREST RIVER — FOREST RIVER ROCKWOOD, FLAGSTAFF
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1166-2017·2017-03-01
Biomet Oxford Partial Knee Instruments Recalled for Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Right Medial Tibial Trial Tray Size B Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1168-2017·2017-03-01
Biomet Recalls Oxford Knee Instruments Due to Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Unicompartmental Knee Phase 3 Shim Size 3 instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Unicompartmental Knee Phase 3 Shim Size 3 Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Food)·F-1514-2017·2017-03-01
Hostess Recalls Holiday White Peppermint Twinkies Due to Salmonella Risk
Hostess Brands is recalling Holiday White Peppermint Twinkies because an ingredient may be contaminated with Salmonella. The product was distributed nationwide.
Product
Holiday White Peppermint Hostess Twinkies, cream-filled snack cakes, Net Wt. 13.02 oz. (369 g), UPC 888109111571.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1155-2017·2017-03-01
Biomet Recalls Oxford Partial Knee Instruments Due to Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Phase 3 Tibial Template Right Medial Size A Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1153-2017·2017-03-01
Biomet Oxford Knee Instruments Recalled for Potential Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Partial Knee System Femoral Slap Hammers due to potential alumina inclusions that could cause the instruments to crack or separate.
Product
Oxford Partial Knee System Femoral Slap Hammer Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1171-2017·2017-03-01
Biomet Oxford Partial Knee Instruments Recalled for Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Phase 3 Tibial Template Right Medial Size D Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1156-2017·2017-03-01
Biomet Oxford Partial Knee Instruments Recalled for Material Inclusions
Biomet U.K. is recalling Oxford Partial Knee instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Right Medial Tibial Trial Tray Size F Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1175-2017·2017-03-01
Biomet Oxford Knee Instruments Recalled for Material Inclusions
Biomet is recalling Oxford Knee instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Phase 3 Tibial Template Right Medial Size B Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1163-2017·2017-03-01
Biomet Recalls Oxford Knee Instruments Due to Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Left Medial Tibial Trial Tray Size D Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
ModerateFDA (Devices)·Z-1245-2017·2017-03-01
Tosoh G8 Reporting Software Recalled Due to Power Outage Shutdowns
Tosoh Smd Inc is recalling 34 units of Reporting Software for the G8 analyzer because power outages cause the software to shut down.
Product
Keyspan High-High Speed USB to Serial Adapter Product Usage: The Reporting Software is an application which serves as middle ware between the Tosoh Automated HPLC G8 analyzer and an LIS or as a stand alone data repository for the analyzer. It is designed to store and manage…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0481-2017·2017-03-01
Sandoz Recalls Transderm Scop Patches Due to Incorrect Labeling Instructions
Sandoz Inc. is recalling Transderm Scop patches because the outer carton contains incorrect instructions for cutting the patch.
Product
Transderm Scop (scopolamine) Transdermal System, 1.5 mg, 1 patch per pouch (NDC 66758-208-58), packaged in 4-count patches per carton (NDC 66758-208-54), Rx Only, Manufactured by ALZA Corporation, Vacaville, CA 95688 for Sandoz Inc., Princeton, NJ 08540.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1250-2017·2017-03-01
Vascular Solutions Recalls GrebSet Micro-Introducer Kits Due to Shelf Life Discrepancy
Vascular Solutions is recalling 633 units of GrebSet Micro-Introducer Kits because the guidewires have a shorter shelf life than the kit expiration date.
Product
GrebSet Micro-Introducer Kit, model 7941, Sterilized with Ethylene Oxide. Product Usage: The GrebSet micro-introducer kit is intended to facilitate the percutaneous placement of guidewires in the vascular system and for delivery of contrast media to vascular sites.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1230-2017·2017-03-01
Cardiovascular Systems Recalls Mislabelled Diamondback 360 Peripheral Atherectomy Components
Cardiovascular Systems Inc is recalling 8 units of the Diamondback 360 Peripheral 1.50 Classic system because a 1.50mm Solid Crown OAD was mislabeled as a 1.50mm Crown OED.
Product
DIAMONDBACK 360 Peripheral 1.50 Classic, Model DBP-150CLASS145 Peripheral Orbital Atherectomy System (OAS) is a minimally invasive, catheter-based OAS designed for improving luminal diameter in patients with peripheral arterial disease (PAD). PAD is caused by the accumulation…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1249-2017·2017-03-01
Durex Condoms Recalled for Missing Benzocaine Labeling Information
Reckitt Benckiser LLC is recalling Durex Pleasure Pack condoms because the package labeling is missing information about the active ingredient Benzocaine.
Product
Durex Pleasure Pack . 3 ultra fine lubricated latex condoms 12 ultra fine lubricated latex condoms 24 Ra fine lubricated latex condoms 3 ct UPC 3-02340-30042-04-1 3 ct - Walmart UPC 02340-70042-04 12ct - UPC 3-02340-30274-08-6 24 ct - UPC 302340-302190-04…
Category
Medical Device
Distribution
Distributed nationwide